FFO — Retractor, Self-Retaining Class I
FDA Device Classification
Classification Details
- Product Code
- FFO
- Device Class
- Class I
- Regulation Number
- 876.4730
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K993544 | advanced surgical concepts (asc) | SPACE-OR RETRACTOR | December 22, 1999 |
| K870897 | sur-med instruments | KODNER ANAL PERIONEAL RETRACTOR | June 4, 1987 |
| K860368 | dantec electronics | URDYN 5000 (UROFLOWMETER) | April 23, 1986 |
| K853119 | dantec electronics | URODYN 1000 | October 4, 1985 |
| K852083 | kendal | THE KENDALL URINARY OUTPUT MONITOR | September 20, 1985 |