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BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1119

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003851
510(k) Type
Traditional
Applicant
BIOCHECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2001
Days to Decision
220 days
Submission Type
Statement

BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1119

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003851
510(k) Type
Traditional
Applicant
BIOCHECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2001
Days to Decision
220 days
Submission Type
Statement