510(k) K874852 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
POLYSTAN WIRE REINFORCED TWO STAGE CATHETERS
| Applicant | Polystan C/O Vitalcor, Inc., Westmont IL, US |
| Decision | Substantially Equivalent, Feb 5, 1988 |
| Received | Nov 25, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874852
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.