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LIQUICHEK SPINAL FLUID CONTROL LEVEL 1, LIQUICHEK SPINAL FLUID CONTROL LEVEL 2, LIQUICHEK SPINAL FLUID CONTROL MINIPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123775
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
52 days
Submission Type
Summary

LIQUICHEK SPINAL FLUID CONTROL LEVEL 1, LIQUICHEK SPINAL FLUID CONTROL LEVEL 2, LIQUICHEK SPINAL FLUID CONTROL MINIPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123775
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2013
Days to Decision
52 days
Submission Type
Summary