510(k) K974285 ยท DPW Flowmeter, Blood, Cardiovascular
PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT
| Applicant | Perimed, Inc., Smithtown NY, US |
| Decision | Substantially Equivalent, May 28, 1998 |
| Received | Nov 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974285
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.