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LIQUICHEK IMMUNOASSAY PLUS CONTROL, MODEL 360, 361, 362, 363

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001373
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2000
Days to Decision
24 days
Submission Type
Summary

LIQUICHEK IMMUNOASSAY PLUS CONTROL, MODEL 360, 361, 362, 363

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001373
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2000
Days to Decision
24 days
Submission Type
Summary