FDA 510(k), K905765, PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)

FDA 510(k), K905765, PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)

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510(K) Number: K905765
Device Name: PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)
Manufacturer: JUDITH A GENZALE
Device Classification Name: Latex Patient Examination Glove
Regulation Number: LYY
Classification Product Code: 12/27/1990
Date Received: 02/25/1991
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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