510(k) K913827 ยท DPW Flowmeter, Blood, Cardiovascular
MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Nov 19, 1991 |
| Received | Aug 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913827
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.