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DOUBLE ANTIBODY ULTRA-PTH #KPTD1 AND KPTD2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871970
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
127 days

DOUBLE ANTIBODY ULTRA-PTH #KPTD1 AND KPTD2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871970
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
127 days