FDA 510(k), K993157, HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240
FDA 510(k), K993157, HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240
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510(K) Number: K993157
Device Name: HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240
Manufacturer: WECK CLOSURE SYSTEMS
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 09/21/1999
Decision Date: 12/17/1999
Regulation Medical Specialty: General & Plastic Surgery
Device Name: HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240
Manufacturer: WECK CLOSURE SYSTEMS
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 09/21/1999
Decision Date: 12/17/1999
Regulation Medical Specialty: General & Plastic Surgery