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Alta Diagnostics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K800327
MAGNESIUM REAGENT
March 25, 1980
K792545
URIC ACID KIT
January 29, 1980
K792546
FETAL CHECK
December 18, 1979
K790796
LIPASE REAGENT SET
July 17, 1979
K790797
AMYLASE REAGENT SET
July 17, 1979