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BETA-HCG MICROTITER PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853258
510(k) Type
Traditional
Applicant
MODERN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1985
Days to Decision
60 days

BETA-HCG MICROTITER PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853258
510(k) Type
Traditional
Applicant
MODERN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1985
Days to Decision
60 days