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FDA 510(k), K042026, BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004
FDA 510(k), K042026, BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004
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510(K) Number: K042026
Device Name: BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 07/28/2004
Decision Date: 09/10/2004
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BARD CK PARASTOMAL HERNIA PATCH, MODELS 0118001, 0118002, 0118003, 0118004
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 07/28/2004
Decision Date: 09/10/2004
Regulation Medical Specialty: General & Plastic Surgery
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