510(k) K944629 ยท GEX Powered Laser Surgical Instrument
MODEL 230-SAC LASER DELIVERY PROBE
| Applicant | Mnlase, Inc., Reston VA, US |
| Decision | Substantially Equivalent, Nov 3, 1994 |
| Received | Sep 20, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944629
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.