FDA 510(k), K922916, BARD MARLEX MESH DART
FDA 510(k), K922916, BARD MARLEX MESH DART
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510(K) Number: K922916
Device Name: BARD MARLEX MESH DART
Manufacturer: CRAIG M AUDET
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 06/17/1992
Date Received: 08/24/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BARD MARLEX MESH DART
Manufacturer: CRAIG M AUDET
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 06/17/1992
Date Received: 08/24/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery