FDA 510(k), K982941, HEM-O-LOK MODEL NUMBERS 523900, 523970
FDA 510(k), K982941, HEM-O-LOK MODEL NUMBERS 523900, 523970
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510(K) Number: K982941
Device Name: HEM-O-LOK MODEL NUMBERS 523900, 523970
Manufacturer: WECK CLOSURE SYSTEMS
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 08/21/1998
Decision Date: 11/19/1998
Regulation Medical Specialty: General & Plastic Surgery
Device Name: HEM-O-LOK MODEL NUMBERS 523900, 523970
Manufacturer: WECK CLOSURE SYSTEMS
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 08/21/1998
Decision Date: 11/19/1998
Regulation Medical Specialty: General & Plastic Surgery