510(k) K920589 ยท GEX Powered Laser Surgical Instrument
ANGLED DELIVERY DEVICE
| Applicant | Laserscope, San Jose CA, US |
| Decision | Substantially Equivalent, Apr 29, 1992 |
| Received | Feb 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920589
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.