510(k) K881521 ยท DXT Injector And Syringe, Angiographic
MODIFIED SERVO SYRINGE
| Applicant | Engineering, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, May 31, 1988 |
| Received | Apr 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881521
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.