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Ezmt Valve Co., 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
K930557
LATEX EXAMINATION GLOVE
September 23, 1993
K930556
NIGHT URINARY DRAINAGE BEDSIDE BAG
May 14, 1993
K913155
LEG URINAL
September 16, 1991