FDA Product Code
FDA Product Code FEI — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Gastroenterology, Urology
- 21 CFR Citation
- 876.1500
510(k) Clearances — 2 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K873795 | M-LENS (THIRTY DEGREE ENDOSCOPE) | Opto Vision, Inc. | 1988-01-14 | Traditional | PDF ↗ |
| K862872 | FLEXIBLE VISUALIZATION CATHETER | American Edwards Laboratories | 1986-10-24 | Traditional | PDF ↗ |
Product code FEI · Class I · Gastroenterology, Urology. Data: openFDA.