510(k) K813231 ยท KCY Tourniquet, Pneumatic
TOURNIQUET
| Applicant | Aspen Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 14, 1981 |
| Received | Nov 17, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813231
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.