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Cooper Medical Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K840144
YAG LASER 8000 GASTROINTESTINAL BLEE
May 18, 1984
K833387
ARGON LASER SURGICAL SYSTEM 770
April 18, 1984
K833497
COOPER MEDICAL MODEL 770
April 17, 1984
K832703
ARGON LASER SYS-MODEL 5000
January 30, 1984
K820261
MONITOR CO2 LASER SYSTEM
March 5, 1982