510(k) K930123 ยท EQH Source, Carrier, Fiberoptic Light
ASPIRATING ENDO OCULAR PROBE
| Applicant | Surgical Technologies, Inc., Chesterfield MO, US |
| Decision | Substantially Equivalent, Feb 16, 1994 |
| Received | Jan 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930123
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.