510(k) K982986 ยท DPW Flowmeter, Blood, Cardiovascular
TUBING BLOOD FLOW METER MODEL NUMBER HD-800
| Applicant | Koven Technology, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Nov 24, 1998 |
| Received | Aug 26, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982986
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.