FDA 510(k), K903607, POWDER FREE, NON-STERILE EXAMINATION GLOVES

FDA 510(k), K903607, POWDER FREE, NON-STERILE EXAMINATION GLOVES

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510(K) Number: K903607
Device Name: POWDER FREE, NON-STERILE EXAMINATION GLOVES
Manufacturer: DEBORAH DENITTO
Device Classification Name: Latex Patient Examination Glove
Regulation Number: LYY
Classification Product Code: 08/07/1990
Date Received: 08/17/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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