K834072 is an FDA 510(k) clearance for the INSTRUMENT, DENTAL. This device is classified as a Curette, Periodontic (Class I — General Controls, product code EMS).
Submitted by Venture Technology, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 21, 1984, 88 days after receiving the submission on November 25, 1983.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K834072 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 25, 1983 |
| Decision Date | February 21, 1984 |
| Days to Decision | 88 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 |