FDA 510(k), K902380, TRIFLEX ORTHOPEDIC STERILE SURGEON'S GLOVE

FDA 510(k), K902380, TRIFLEX ORTHOPEDIC STERILE SURGEON'S GLOVE

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510(K) Number: K902380
Device Name: TRIFLEX ORTHOPEDIC STERILE SURGEON'S GLOVE
Manufacturer: A CAMPBELL
Device Classification Name: Surgeon'S Gloves
Regulation Number: KGO
Classification Product Code: 05/30/1990
Date Received: 06/18/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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