510(k) K931072 ยท HJM Transilluminator, Ac-Powered
HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE
| Applicant | Hgm, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 10, 1994 |
| Received | Mar 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931072
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.