510(k) K864259 ยท DPW Flowmeter, Blood, Cardiovascular
MODIFIED LASERFLO BLOOD PERFUSION MONITOR
| Applicant | Tsi, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Feb 20, 1987 |
| Received | Oct 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864259
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.