510(k) K922368 ยท DPW Flowmeter, Blood, Cardiovascular
PERIFLUX PF4001 LASER DOPPLER FLOWMETER
| Applicant | Perimed, Inc., Piscataway NJ, US |
| Decision | Substantially Equivalent, Feb 3, 1993 |
| Received | May 20, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922368
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.