510(k) K981277 ยท HIR Perineometer
PERIFORM
| Applicant | Verimed Holdings, Inc., Coral Springs FL, US |
| Decision | Substantially Equivalent, Nov 20, 1998 |
| Received | Apr 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981277
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.