FDA 510(k), K070026, POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES

FDA 510(k), K070026, POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES

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510(K) Number: K070026
Device Name: POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES
Manufacturer: KATHY LIU
Device Classification Name: Vinyl Patient Examination Glove
Regulation Number: LYZ
Classification Product Code: 01/03/2007
Date Received: 03/07/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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