FDA 510(k), K083752, GLUSEAL 90, MODEL GLU9010
FDA 510(k), K083752, GLUSEAL 90, MODEL GLU9010
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$149.00 USD
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510(K) Number: K083752
Device Name: GLUSEAL 90, MODEL GLU9010
Manufacturer: GLUSTITCH, INC.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 12/17/2008
Decision Date: 02/23/2009
Regulation Medical Specialty: General Hospital
Device Name: GLUSEAL 90, MODEL GLU9010
Manufacturer: GLUSTITCH, INC.
Device Classification Name: bandage, liquid
Regulation Number: 880.5090
Classification Product Code: KMF
Date Received: 12/17/2008
Decision Date: 02/23/2009
Regulation Medical Specialty: General Hospital