Last synced on 25 January 2026 at 3:41 am

LIQUICHECK URINALYSIS CONTROL BILEVEL, MODEL 435, LIQUICHEK URINALYSIS CONTROL LEVEL 2, MODEL 436, LIQUICHEK URINALYSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031231
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2003
Days to Decision
61 days
Submission Type
Summary

LIQUICHECK URINALYSIS CONTROL BILEVEL, MODEL 435, LIQUICHEK URINALYSIS CONTROL LEVEL 2, MODEL 436, LIQUICHEK URINALYSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031231
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2003
Days to Decision
61 days
Submission Type
Summary