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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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