510(k) K904317 ยท DPW Flowmeter, Blood, Cardiovascular
AVALON GENERAL PURPOSE SCANNER, PREVIEW GP
| Applicant | Avalon Technology Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 13, 1991 |
| Received | Sep 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904317
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.