510(k) K896435 ยท DPT Probe, Blood-Flow, Extravascular
HP SONOS 500 AND SONOS 1000 ULTRA. IMAGING SYSTEM
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Feb 7, 1990 |
| Received | Nov 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896435
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.