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Diatron U.S., Inc.

FDA Regulatory Profile

Diatron U.S., Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 14, 2016.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151487Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase MethodJanuary 14, 2016
K111534ABACUS 3CPAugust 2, 2012
K112755ABACUS 5March 27, 2012

FDA data resources