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Orotracheal Intubation Guide Kit
FDA product code OGK · Class 2 · Anesthesiology
16
Registered devices
3
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Intubation Guide Kit — Nar Medical Depot, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCIntubation Guide Kit — Nar Medical Depot, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCDeRoyal — DEROYAL INDUSTRIES, INC.Curaplex — BOUND TREE MEDICAL, LLCACS — AMERICAN CONTRACT SYSTEMS, INC.Curaplex — BOUND TREE MEDICAL, LLCIntubation Guide Kit — Nar Medical Depot, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-08-04 | Smiths Medical ASD Inc. | The incorrect device is contained in the package. |
| 2012-06-18 | superDimension, Inc | superDimension, Inc., is conducting a recall of certain superDimension Systems operating Software Version 4.0 - 4.9. The affected systems are sold under the pr |
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