510(k) K910049 ยท DPW Flowmeter, Blood, Cardiovascular
INTERSPEC APOGEE, MODIFICATION
| Applicant | Interspec, Inc., Ambler PA, US |
| Decision | Substantially Equivalent, Apr 29, 1991 |
| Received | Jan 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910049
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.