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FDA 510(k), K103767, DUAL HEATED INFANT VREATHING CIROUITS
FDA 510(k), K103767, DUAL HEATED INFANT VREATHING CIROUITS
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510(K) Number: K103767
Device Name: DUAL HEATED INFANT VREATHING CIROUITS
Manufacturer: FISHER & PAYKEL HEALTHCARE LTD.
Device Classification Name: heater, breathing system w/wo controller (not humidifier or nebulizer
Regulation Number: 868.5270
Classification Product Code: BZE
Date Received: 12/23/2010
Decision Date: 04/16/2012
Regulation Medical Specialty: Anesthesiology
Device Name: DUAL HEATED INFANT VREATHING CIROUITS
Manufacturer: FISHER & PAYKEL HEALTHCARE LTD.
Device Classification Name: heater, breathing system w/wo controller (not humidifier or nebulizer
Regulation Number: 868.5270
Classification Product Code: BZE
Date Received: 12/23/2010
Decision Date: 04/16/2012
Regulation Medical Specialty: Anesthesiology
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- Delivery: Approximately 1 to 2 weeks
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