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LIQUICHEK RHEUMATOID FACTOR CONTROL

Page Type
Cleared 510(K)
510(k) Number
K960987
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1996
Days to Decision
85 days
Submission Type
Summary

LIQUICHEK RHEUMATOID FACTOR CONTROL

Page Type
Cleared 510(K)
510(k) Number
K960987
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1996
Days to Decision
85 days
Submission Type
Summary