510(k) K801173 ยท KRA Catheter, Continuous Flush
ANGIO-FLO MONITORING KIT
| Applicant | Hospital Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, May 28, 1980 |
| Received | May 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801173
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.