510(k) K893816 ยท LYK Angioscope
HEMOLASER HEMOSCOPE
| Applicant | Hemolaser Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 1, 1990 |
| Received | May 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893816
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.