510(k) K981191 ยท DQY Catheter, Percutaneous
ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65
| Applicant | Intratherapeutics, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Apr 7, 1999 |
| Received | Apr 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981191
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.