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MODIFICATION TO API UNISCEPT 20GP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901559
510(k) Type
Traditional
Applicant
ANALYTICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
160 days

MODIFICATION TO API UNISCEPT 20GP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901559
510(k) Type
Traditional
Applicant
ANALYTICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
160 days