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SOPHEIA DIGITOXIN EIA KIT & COMPONENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830035
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/1983
Days to Decision
21 days

SOPHEIA DIGITOXIN EIA KIT & COMPONENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830035
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/1983
Days to Decision
21 days