510(k) K942303 ยท KCY Tourniquet, Pneumatic
TECNADYNE T-CUFF
| Applicant | Technadyne Scientific, Inc., Vero Beach FL, US |
| Decision | Substantially Equivalent, Jul 20, 1994 |
| Received | May 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942303
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.