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MODIFIED D-DI-TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890399
510(k) Type
Traditional
Applicant
AMERICAN BIOPRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1989
Days to Decision
14 days

MODIFIED D-DI-TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890399
510(k) Type
Traditional
Applicant
AMERICAN BIOPRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1989
Days to Decision
14 days