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HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES

Page Type
Cleared 510(K)
510(k) Number
K890281
510(k) Type
Traditional
Applicant
CAMBRIDGE BIOSCIENCE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1989
Days to Decision
57 days

HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES

Page Type
Cleared 510(K)
510(k) Number
K890281
510(k) Type
Traditional
Applicant
CAMBRIDGE BIOSCIENCE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1989
Days to Decision
57 days