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Denka Seiken'S

FDA Regulatory Profile

Denka Seiken'S appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 27, 2002.

Summary

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

Known Names

denka seiken, denka seiken co

Recent 510(k) Clearances

K-NumberDeviceDate
K011400MRSA-SCREENMarch 27, 2002
K013359LP(A)-LATEX SEIKEN ASSAY KITMarch 8, 2002
K011958CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KITDecember 4, 2001
K981734VTEC-RPLA SEIKENSeptember 22, 1998

FDA data resources