FDA 510(k), K972446, PEDO CUSH PEDO CUDDLE

FDA 510(k), K972446, PEDO CUSH PEDO CUDDLE

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510(K) Number: K972446
Device Name: PEDO CUSH PEDO CUDDLE
Manufacturer:
Device Classification Name: Restraint, Protective
Regulation Number: 880.6760
Classification Product Code: FMQ
Date Received: 06/30/1997
Decision Date: 11/13/1997
Regulation Medical Specialty: General Hospital
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