National Advanced Endoscopy Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K170285 | AED Sinuscope | August 1, 2017 |
| K141515 | AED HYSTEROSCOPE AND ACCESSORIES | January 7, 2015 |
| K102663 | AED RESECTOSCOPE | December 30, 2010 |
| K081553 | AED BIPOLAR FORCEPS, MODEL 13-1646 | September 29, 2008 |
| K081503 | AED MONOPOLAR LAP ACCESSORIES | September 25, 2008 |
| K993689 | AED CYSTOSCOPE | December 15, 1999 |
| K993688 | AED LAPAROSCOPE | December 6, 1999 |
| K991656 | AED ARTHROSCOPE | December 2, 1999 |