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Siemens Helathcare Diagnostics, Inc.

FDA Regulatory Profile

Siemens Helathcare Diagnostics, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 8, 2013.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131275MICROSCAN DRIED GRAM-POSTIVE MIC/COMBO PANELSNovember 8, 2013
K132391IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VESeptember 20, 2013

FDA data resources