Home › Device types › KQG
Instrument, Coagulation
FDA product code KQG · Class 2 · Hematology
0
Registered devices
39
Adverse events
1
Recalls
14
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-11-30 | International Technidyne Corp. | Some Activated Clotting Time (ACT) Tubes may contain a component that does not meet its specification, making it possible for a failure to detect a tube or the |
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