510(k) K950118 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ABRM CATHETER
| Applicant | Cook, Inc., Bloomington IN, US |
| Decision | Substantially Equivalent, Feb 8, 1996 |
| Received | Jan 11, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950118
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 16, 2007 | Cook, Inc. COOK Triple Lumen Central Venous Catheter Tray with Cook Spectrum Glide Antimicrobial Catheter with EZ--Pass Hydrophilic Coating: Reorder Number C-UTLMY-701J-RSC-ABRM-HC-FST-A. Terminated |
FOZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.