Submission Details
| 510(k) Number | K851721 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 25, 1985 |
| Decision Date | July 02, 1985 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
K851721 is an FDA 510(k) clearance for the 1200/1 TO 1240/15 VARIOUS TYPES OF DENTAL SCALERS, a Scaler, Periodontic (Class I — General Controls, product code EMN), submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on July 2, 1985, 68 days after receiving the submission on April 25, 1985. This device falls under the Dental review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K851721 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 25, 1985 |
| Decision Date | July 02, 1985 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EMN — Scaler, Periodontic |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 872.4565 |