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Buhlmann Laboratories AG

FDA Regulatory Profile

Buhlmann Laboratories AG appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 24, 2019.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K191718Buhlmann fCAL turbo and CALEX CapSeptember 24, 2019
K190784BUHLMANN fCAL turboJune 25, 2019
K181012BUHLMANN fCAL ELISAJune 4, 2018
K954299BUHLMANN ANGIOSTENSIN II RIAOctober 19, 1995

FDA data resources