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LIQUID CSF(LCR)1, LIQUID CSF(LCR)2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970979
510(k) Type
Traditional
Applicant
CHIRON DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1997
Days to Decision
16 days
Submission Type
Statement

LIQUID CSF(LCR)1, LIQUID CSF(LCR)2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970979
510(k) Type
Traditional
Applicant
CHIRON DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1997
Days to Decision
16 days
Submission Type
Statement