Submission Details
| 510(k) Number | K925370 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 23, 1992 |
| Decision Date | March 18, 1993 |
| Days to Decision | 146 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
K925370 is an FDA 510(k) clearance for the TRIANGULAR JAW MICROLARYNGEAL FORCEPS, a Material, Impression (Class II — Special Controls, product code ELW), submitted by Pilling Co. (Fort Washington, US). The FDA issued a Cleared decision on March 18, 1993, 146 days after receiving the submission on October 23, 1992. This device falls under the Dental review panel. Regulated under 21 CFR 872.3660.
| 510(k) Number | K925370 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 23, 1992 |
| Decision Date | March 18, 1993 |
| Days to Decision | 146 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | ELW — Material, Impression |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3660 |