Model Fbs-1, Flexible Bronchoscope
K811181 is the FDA 510(k) clearance record for MODEL FBS-1, FLEXIBLE BRONCHOSCOPE, a class II device, cleared for American Optical Corp. on under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)). FDA's definition for product code EOQ reads: "A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the...". FDA records list 35 510(k) clearances for American Optical Corp., from to . As of , FDA records show no recalls naming K811181.
Clearance record
- Decision date
- Received
- (15 days to decision)
- Product code
- EOQ Bronchoscope (Flexible Or Rigid)
- Regulation
- 21 CFR 874.4680
- Device class
- Class II
- Review panel
- Ear, Nose, Throat
- Applicant
- American Optical Corp. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code EOQ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 2 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 2 |
| August 2026 | 0 |
| September 2026 | 3 |
| October 2026 | 0 |
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