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Medmark, 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
K914498
POWDER FREE, NON-STERILE, LATEX EXAMINATION GLOVES
November 27, 1991
K894987
MODEL #520/525 ED/RECOVERY STRETCHER
September 5, 1989
K893949
#157 EXAM LIGHT
August 7, 1989