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IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN

Page Type
Cleared 510(K)
510(k) Number
K831961
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
55 days

IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN

Page Type
Cleared 510(K)
510(k) Number
K831961
510(k) Type
Traditional
Applicant
KENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
55 days