FDA 510(k), K003335, RESUSCITAIRE RADIANT WARMER; RESUSCITAIRE BIRTHING ROOM WARMER; RESUSCITAIR WALL MOUNTED RADIANT WARMER

FDA 510(k), K003335, RESUSCITAIRE RADIANT WARMER; RESUSCITAIRE BIRTHING ROOM WARMER; RESUSCITAIR WALL MOUNTED RADIANT WARMER

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510(K) Number: K003335
Device Name: RESUSCITAIRE RADIANT WARMER; RESUSCITAIRE BIRTHING ROOM WARMER; RESUSCITAIR WALL MOUNTED RADIANT WARMER
Manufacturer:
Device Classification Name: Warmer, Infant Radiant
Regulation Number: 880.5130
Classification Product Code: FMT
Date Received: 10/25/2000
Decision Date: 11/17/2000
Regulation Medical Specialty: General Hospital
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