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LIQUICHEK HEMATOLOGY-16 CONTROL LV, MODEL: 295LV

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091303
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2010
Days to Decision
455 days
Submission Type
Summary

LIQUICHEK HEMATOLOGY-16 CONTROL LV, MODEL: 295LV

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091303
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2010
Days to Decision
455 days
Submission Type
Summary