FEI — Instrument, Special Lens, For Endoscope Class I
FDA Device Classification
Classification Details
- Product Code
- FEI
- 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 |
|---|
| K873795 | opto vision | M-LENS (THIRTY DEGREE ENDOSCOPE) | January 14, 1988 |
| K862872 | american edwards laboratories | FLEXIBLE VISUALIZATION CATHETER | October 24, 1986 |