510(k) K014002 ยท KOB Catheter, Suprapubic (And Accessories)
ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890
| Applicant | Fortune Medical Instrument Corp., Taipei Hsien, TW |
| Decision | Substantially Equivalent, Mar 4, 2002 |
| Received | Dec 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014002
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.