K832899 is an FDA 510(k) clearance for the ZIMMER OSSIMETER. This device is classified as a Tape, Measuring, Rulers And Calipers (Class I - General Controls, product code FTY).
Submitted by Zimmer, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 14, 1983, 46 days after receiving the submission on August 29, 1983.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K832899 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 29, 1983 |
| Decision Date | October 14, 1983 |
| Days to Decision | 46 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | FTY — Tape, Measuring, Rulers And Calipers |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4800 |