510(k) K851057 ยท DPW Flowmeter, Blood, Cardiovascular
LASERFLO BLOOD PERFUSION MONITOR 403
| Applicant | Tsi, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jun 24, 1985 |
| Received | Mar 14, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851057
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.