FEJ — Attachment, Binocular, For Endoscope Class I
FDA product code FEJ covers "Attachment, Binocular, For Endoscope", a Class I medical device regulated under 21 CFR 876.1500. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- FEJ
- Device Class
- Class I
- Regulation Number
- 876.1500
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K840837 | manico | TBI TRAINER | March 25, 1985 |