510(k) K933994 ยท KCY Tourniquet, Pneumatic
ARTHREX TOURNIQUET FOR LEG HOLDER
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 23, 1994 |
| Received | Aug 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933994
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.