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FDA 510(k), K781232, IPPB ASSEMBLY W/NEBULIZER
FDA 510(k), K781232, IPPB ASSEMBLY W/NEBULIZER
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510(K) Number: K781232
Device Name: IPPB ASSEMBLY W/NEBULIZER
Manufacturer:
Device Classification Name: Device, Positive Pressure Breathing, Intermittent
Regulation Number: NHJ
Classification Product Code: KXA
Date Received: 07/21/1978
Decision Date: 09/27/1978
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: IPPB ASSEMBLY W/NEBULIZER
Manufacturer:
Device Classification Name: Device, Positive Pressure Breathing, Intermittent
Regulation Number: NHJ
Classification Product Code: KXA
Date Received: 07/21/1978
Decision Date: 09/27/1978
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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