FDP — Apparatus, Pneumoperitoneum, Automatic Class II
FDA product code FDP covers "Apparatus, Pneumoperitoneum, Automatic", a Class II 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
- FDP
- Device Class
- Class II
- Regulation Number
- 876.1500
- Submission Type
- Review Panel
- SU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K910875 | ethicon | ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE | March 19, 1991 |