510(k) K840590 ยท HQF Laser, Ophthalmic
FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE
| Applicant | Hgm, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 9, 1984 |
| Received | Feb 9, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840590
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.