Cathaid, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K864115TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SUNovember 7, 1986
K863958TUBEGRIPPER, UROLOGICAL CATHETER & ACCESSORYNovember 4, 1986
K863957TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR GUOctober 24, 1986