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B2 MICROGLOBULIN ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K964791
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1997
Days to Decision
181 days
Submission Type
Summary

B2 MICROGLOBULIN ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K964791
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1997
Days to Decision
181 days
Submission Type
Summary