K951529 is an FDA 510(k) clearance for the V. MUELLER OBSTETRICAL (OB) FORCEPS. This device is classified as a Forceps, Obstetrical (Class II - Special Controls, product code HDA).
Submitted by Baxter Healthcare Corp (Waukegan, US). The FDA issued a Cleared decision on August 4, 1995, 123 days after receiving the submission on April 3, 1995.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.4400.
| 510(k) Number | K951529 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 03, 1995 |
| Decision Date | August 04, 1995 |
| Days to Decision | 123 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HDA — Forceps, Obstetrical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.4400 |