510(k) K910512 ยท KCY Tourniquet, Pneumatic
ACCUFLATE
| Applicant | Instrumed, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Feb 19, 1991 |
| Received | Feb 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910512
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.