510(k) K963204 ยท GFE Brush, Dermabrasion, Powered
DMS-1000C DERMOABRADER
| Applicant | Aesthetic Lasers, Inc., Annapolis MD, US |
| Decision | Substantially Equivalent, Dec 9, 1996 |
| Received | Aug 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963204
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.