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LIQUICHEK AUTOIMMUNE NEGATIVE CONTROL, CATALOG #130

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024220
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2003
Days to Decision
25 days
Submission Type
Summary

LIQUICHEK AUTOIMMUNE NEGATIVE CONTROL, CATALOG #130

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024220
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2003
Days to Decision
25 days
Submission Type
Summary