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

Page Type
Cleared 510(K)
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)
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