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Laryngoscope Kit
FDA product code OGH · Class 1 · Anesthesiology
69
Registered devices
18
Adverse events
4
Recalls
0
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCEmergency Medical Products — EMERGENCY MEDICAL PRODUCTS, INC.Ambu® SureSight® Mobile Kit — Ambu A/SRingLoc Hip System — Biomet Orthopedics, LLCIntegra® MicroFrance® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCKing Vision Video Laryngoscope Kit — King Systems CorporationCARDINAL HEALTH — Cardinal Health 200, LLCACS — AMERICAN CONTRACT SYSTEMS, INC.Curaplex — BOUND TREE MEDICAL, LLCACS — AMERICAN CONTRACT SYSTEMS, INC.RingLoc Hip System — Biomet Orthopedics, LLCCARDINAL HEALTH — Cardinal Health 200, LLCRingLoc Hip System — Biomet Orthopedics, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCuraplex — BOUND TREE MEDICAL, LLCCuraplex — BOUND TREE MEDICAL, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCuraplex — BOUND TREE MEDICAL, LLCACS — AMERICAN CONTRACT SYSTEMS, INC.Integra® MicroFrance® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCAmbu® SureSight® Mobile Mini Kit — Ambu A/SCARDINAL HEALTH — Cardinal Health 200, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-08 | Cardinal Health 200, LLC | Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits. |
| 2024-11-08 | Cardinal Health 200, LLC | Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits. |
| 2019-11-27 | Flexicare Medical Ltd. | The firm has received reports that the spring/washer/bearing components in the block of the laryngoscope blade become loose and separated from the device. If t |
| 2019-11-27 | Flexicare Medical Ltd. | The firm has received reports that the spring/washer/bearing components in the block of the laryngoscope blade become loose and separated from the device. If t |
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