510(k) K860095 ยท KCY Tourniquet, Pneumatic
DIGIKIT NONPNEUMATIC TOURNIQUET
| Applicant | Orthofab, Inc., Cottage Grove MN, US |
| Decision | Substantially Equivalent, Jan 24, 1986 |
| Received | Jan 10, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860095
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.