510(k) K860463 ยท KCY Tourniquet, Pneumatic
SINGLE AND DUAL TOURNIQUET CUFF
| Applicant | Aspen Laboratories, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Feb 25, 1986 |
| Received | Feb 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860463
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.