510(k) K942381 ยท DXT Injector And Syringe, Angiographic
LOW PRESSURE INJECTION TUBING, COILED LINE, EXTENSION TUBING
| Applicant | Apogee, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Mar 17, 1995 |
| Received | May 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942381
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.