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FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K992436
GOWN BACK, MODEL 13-403N; 13-404N; 13-405N
January 20, 2000
K920045
DURATECH HOSPITAL TOWEL
July 2, 1992
K920153
THERMUFF BAG
July 1, 1992