Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
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
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