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LIQUICHEK SPINAL FLUID CONTROL LEVELS I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932076
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/1993
Days to Decision
61 days
Submission Type
Statement

LIQUICHEK SPINAL FLUID CONTROL LEVELS I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932076
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/1993
Days to Decision
61 days
Submission Type
Statement