510(k) K922787 ยท DQX Wire, Guide, Catheter
ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION
| Applicant | Echocath, Inc., Princeton NJ, US |
| Decision | Substantially Equivalent, Jan 6, 1993 |
| Received | Jun 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922787
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.