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Comeg Endoscopy
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K971881
COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTO
August 12, 1997
K970764
COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES
April 22, 1997
K970489
COMEG ENDOSCOPY GRASPING FORCEPS
March 19, 1997