K833288 is an FDA 510(k) clearance for the C & B57 PENTRON C & B57. This device is classified as a Remover, Crown (Class I - General Controls, product code EIS).
Submitted by Genesis Industries, Inc. (Walker, US). The FDA issued a Cleared decision on December 20, 1983, 89 days after receiving the submission on September 22, 1983.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K833288 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 22, 1983 |
| Decision Date | December 20, 1983 |
| Days to Decision | 89 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EIS — Remover, Crown |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |