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BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001022
510(k) Type
Traditional
Applicant
Biocheck, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2000
Days to Decision
180 days
Submission Type
Statement

BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001022
510(k) Type
Traditional
Applicant
Biocheck, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2000
Days to Decision
180 days
Submission Type
Statement