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MODIFICATION TO LIQUICHEK SPINAL FLUID CONTROL, ITEM NOS. 751, 752

Page Type
Cleared 510(K)
510(k) Number
K990888
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1999
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO LIQUICHEK SPINAL FLUID CONTROL, ITEM NOS. 751, 752

Page Type
Cleared 510(K)
510(k) Number
K990888
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1999
Days to Decision
28 days
Submission Type
Summary