510(k) K884354 ยท DQO Catheter, Intravascular, Diagnostic
IMAGER FLUSH CATHETERS
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Apr 21, 1989 |
| Received | Oct 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884354
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.