510(k) K972575 ยท GEX Powered Laser Surgical Instrument
800 SERIES SURGICAL LASER SYSTEM ORION SERIES SURGICAL LASER SYSTEM ANGLED DELIVERY DEVICES
| Applicant | Laserscope, San Jose CA, US |
| Decision | Substantially Equivalent, Jul 17, 1998 |
| Received | Jul 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972575
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.