510(k) K960521 ยท GEX Powered Laser Surgical Instrument
SHARPLAN LASERS, INC. SILKTOUCH FLASH SCANNER
| Applicant | Sharplan Lasers, Inc., Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 26, 1996 |
| Received | Feb 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960521
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.