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N-ASSAY TIA MICROALBUMIN CALIBRATOR SET

Page Type
Cleared 510(K)
510(k) Number
K934143
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
73 days
Submission Type
Statement

N-ASSAY TIA MICROALBUMIN CALIBRATOR SET

Page Type
Cleared 510(K)
510(k) Number
K934143
510(k) Type
Traditional
Applicant
CRESTAT DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
73 days
Submission Type
Statement