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Cathaid, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K864115
TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU
November 7, 1986
K863958
TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORY
November 4, 1986
K863957
TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR GU
October 24, 1986