510(k) K971935 ยท JBP Activated Whole Blood Clotting Time
B&D ACTIVATED CLOTTING TIME (ACT) TEST TUBES BD-C101 (DIATOMACEOUS EARTH) AND BD-K101 (KAOLIN)
| Applicant | B & D Corp., Metuchen NJ, US |
| Decision | Substantially Equivalent, Oct 1, 1997 |
| Received | May 27, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971935
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.