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Glederer & Co., Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K955661
ACU-HALT
December 30, 1996
K955776
ACU-LAB
June 5, 1996