510(k) K902263 ยท GGX Pipette, Sahli
OPTILASE MODEL 1000 ND:YAG LASER ADD'L INDICATION
| Applicant | Trimedyne, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jul 23, 1990 |
| Received | May 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902263
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.