Product code EOQ: 510(k) clearances and predicates
Product code EOQ covers Single-use Flexible Bronchoscope. FDA lists 244 clearances under this code in the 510(k) index. This page summarizes recent clearance volume and names recent clearances by K number so you can pick predicates faster.
Clearance volume
244 clearances on file under product code EOQ. Counts by year:
| Year | Clearances |
|---|---|
| 2022 | 11 |
| 2023 | 12 |
| 2024 | 13 |
| 2025 | 20 |
| 2026 so far | 9 |
Recent clearances
Newest EOQ clearances in the FDA index, with applicant and decision date:
- K261637, Single-use Flexible Bronchoscope, applicant Hunan Vathin Medical Instrument Co., Ltd., decided 2026-09-23. FDA record
- K260309, Ambu® aScope 5 Broncho 2.7/1.2; Ambu® aScope 5 Broncho 4.2/2.2; Ambu® aScope 5 Broncho 4.2/2.2 Sampler Set, applicant Ambu A/S, decided 2026-09-16. FDA record
- K254026, 3.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U), applicant Flexicare Medical Limited., decided 2026-09-02. FDA record
- K260382, MONARCH Platform (MON-000008), applicant Auris Health, Inc., decided 2026-07-25. FDA record
- K254037, LungFlow Airway Catheter, applicant Free Flow Medical, Inc., decided 2026-07-10. FDA record
- K253137, FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840T, applicant Fujifilm Corporation, decided 2026-06-16. FDA record
- K260565, SmartClip Delivery Catheter (ADR-1715), applicant Elucent Medical, decided 2026-05-14. FDA record
- K252341, EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-Q190); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-H190 ); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH190), applicant Olympus Medical Systems Corp., decided 2026-04-23. FDA record
What this means for a regulatory watcher
Volume tells you how deep the predicate pool is. A code with steady yearly counts gives you many candidate predicates, which helps when one predicate has a recall or design gap. A code with a sharp recent rise means reviewers are seeing more of this device type, so substantial equivalence arguments need to track the newest cleared devices, not five year old ones. Related device names in recent clearances include Ambu® aScope 5 Broncho 2.7/1.2; Ambu® aScope 5 Broncho 4.2/2.2; Ambu® aScope 5 Broncho 4.2/2.2 Sampler Set, 3.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U). Watch new EOQ clearances as they post: each one is a possible predicate for your submission and a possible competitor worth reading.
FAQ
What is FDA product code EOQ?
It is the three letter code FDA assigns to a device type in the 510(k) index. Recent EOQ clearances include Single-use Flexible Bronchoscope.
How many 510(k) clearances use product code EOQ?
244 at the time this page was generated, from openFDA records.
How do I find a predicate device under EOQ?
Start with the recent K numbers listed above, then run the free predicate search to check substantial equivalence text and review history.
How do I track new EOQ clearances?
Get 510(k) alerts filtered to this product code and read each new clearance as it posts.
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Data: U.S. FDA via openFDA (public domain). Not regulatory advice. Assume all results are unvalidated.