510(k) K935081 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
DIRECTDRAW SUPERSERUM-MINI
| Applicant | International Technidyne Corp., Edison NJ, US |
| Decision | Substantially Equivalent, Jan 11, 1994 |
| Received | Oct 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935081
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.