510(k) K924273 ยท KCY Tourniquet, Pneumatic
ACCUFLATE
| Applicant | Instrumed, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Jan 12, 1993 |
| Received | Aug 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924273
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 18, 2011 | Stryker Instruments Div. of Stryker Corporation Stryker Instruments, SmartPump Tourniquet System, Dual Channel Tourniquet Pump, REF 5920-011-000, Rx only.
Intended to be used to temporarily occlude or decrease blood flow in a patient extremity duri Terminated |
KCY | None listed |
| Jan 18, 2011 | Stryker Instruments Div. of Stryker Corporation Stryker Instruments, SmartPump Tourniquet System, Single Channel Tourniquet Pump, REF 5920-010-000, Rx only, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
Intended t Terminated |
KCY | None listed |
| Jan 18, 2011 | Stryker Instruments Div. of Stryker Corporation Stryker Instruments, SmartPump Tourniquet System, Report Printer Kit, REF 5920-012-000, Rx only, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
Provides a record of a Terminated |
KCY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.