K894663 is an FDA 510(k) clearance for the BEAMER ONE. This device is classified as a Apparatus, Electrosurgical (Class II - Special Controls, product code HAM).
Submitted by Beacon Laboratories, Inc. (Westminster, US). The FDA issued a Cleared decision on September 15, 1989, 53 days after receiving the submission on July 24, 1989.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4400.
| 510(k) Number | K894663 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 24, 1989 |
| Decision Date | September 15, 1989 |
| Days to Decision | 53 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | HAM — Apparatus, Electrosurgical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4400 |