510(k) K880777 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
8.5 FR. PESCUTANEOUS SHEATH INTRODUCER SYSTEM
| Applicant | Medsurg Industries, Inc., Herndon VA, US |
| Decision | Substantially Equivalent, May 24, 1988 |
| Received | Feb 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880777
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.