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ANTITHROMBIN III ASSAY

Page Type
Cleared 510(K)
510(k) Number
K780002
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1978
Days to Decision
32 days

ANTITHROMBIN III ASSAY

Page Type
Cleared 510(K)
510(k) Number
K780002
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1978
Days to Decision
32 days