Last synced on 14 November 2025 at 11:06 pm

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

Page Type
Cleared 510(K)
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)
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