510(k) K903838 ยท GEX Powered Laser Surgical Instrument
OPTILASE (TM) MODEL 900 ARGON
| Applicant | Trimedyne, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Mar 5, 1991 |
| Received | Aug 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903838
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.