510(k) K921320 ยท GEX Powered Laser Surgical Instrument
ELIOS DIODE OPHTHALMIC LASER
| Applicant | Marco Ophthalmic, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jul 2, 1992 |
| Received | Mar 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921320
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.