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Safeway Products, 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
K891508
PATIENT EXAMINATION GLOVES (LATEX)
April 6, 1989
K862811
AQUALUX LENS CASE
September 3, 1986
K822828
SOFT LENS THERMAL DISINFECTING UNIT, A-C
October 29, 1982