Submission Details
| 510(k) Number | K843233 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 17, 1984 |
| Decision Date | October 25, 1984 |
| Days to Decision | 69 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
K843233 is an FDA 510(k) clearance for the ANATOM SYSTEM. This device is classified as a Chair, Dental, With Operative Unit (Class I — General Controls, product code KLC).
Submitted by Lic-Orthion (Washington, US). The FDA issued a Cleared decision on October 25, 1984, 69 days after receiving the submission on August 17, 1984.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6250.
| 510(k) Number | K843233 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 17, 1984 |
| Decision Date | October 25, 1984 |
| Days to Decision | 69 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | KLC — Chair, Dental, With Operative Unit |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 872.6250 |