510(k) K860358 ยท HQF Laser, Ophthalmic
FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE)
| Applicant | Hgm, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 21, 1986 |
| Received | Jan 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860358
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.