510(k) K990725 ยท GEX Powered Laser Surgical Instrument
NUVOLASE 532 LASER SYSTEM
| Applicant | American Laser Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 22, 1999 |
| Received | Mar 5, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990725
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.