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IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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