510(k) K001198 ยท DQX Wire, Guide, Catheter
DATASCOPE NITINOL CATHETER GUIDE WIRE (145 CM), DATASCOPE NITINOL CATHETER GUIDE WIRE (175 CM), DATASCOPE NITINOL CATHET
| Applicant | Datascope Corp., Fairfield NJ, US |
| Decision | Substantially Equivalent, May 12, 2000 |
| Received | Apr 13, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001198
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.