510(k) K992622 ยท DQY Catheter, Percutaneous
INTRAMAX ITI GUIDE CATHETER
| Applicant | Intratherapeutics, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Sep 29, 1999 |
| Received | Aug 5, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992622
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.