FDA 510(k), K003337, HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240

510(K) Number: K003337
Device Name: HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240
Manufacturer:
Device Classification Name: Clip, Implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 10/25/2000
Decision Date: 12/21/2000
Regulation Medical Specialty: General & Plastic Surgery