510(k) K862251 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter
MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE
| Applicant | Bio-Flow, Inc., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Sep 4, 1986 |
| Received | Jun 12, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862251
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.