510(k) K864810 ยท HMP Pad, Eye
LIDSPLINT
| Applicant | Precision Therapeutics, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jan 20, 1987 |
| Received | Dec 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864810
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.