K872091 is an FDA 510(k) clearance for the CURRETTES, ALVEOLAR (MOLT AND MILLER). This device is classified as a Curette, Periodontic (Class I - General Controls, product code EMS).
Submitted by Military Engineering, Inc. (Plymouth, US). The FDA issued a Cleared decision on July 31, 1987, 60 days after receiving the submission on June 1, 1987.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K872091 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 01, 1987 |
| Decision Date | July 31, 1987 |
| Days to Decision | 60 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EMS — Curette, Periodontic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |