510(k) K954934 ยท GEX Powered Laser Surgical Instrument
CANDELA SPTL LONG PULSE/TUNABLE PULSED DYE LASE
| Applicant | Candela Laser Corp., Washington DC, US |
| Decision | Substantially Equivalent, Feb 2, 1996 |
| Received | Oct 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954934
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.