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HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES

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