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CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011958
510(k) Type
Traditional
Applicant
DENKA SEIKEN'S
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/4/2001
Days to Decision
165 days
Submission Type
Summary

CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011958
510(k) Type
Traditional
Applicant
DENKA SEIKEN'S
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/4/2001
Days to Decision
165 days
Submission Type
Summary