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LIQUICHEK RHEUMATOID FACTOR CONTROL

Page Type
Cleared 510(K)
510(k) Number
K923578
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1992
Days to Decision
78 days
Submission Type
Statement

LIQUICHEK RHEUMATOID FACTOR CONTROL

Page Type
Cleared 510(K)
510(k) Number
K923578
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1992
Days to Decision
78 days
Submission Type
Statement