Last synced on 14 November 2025 at 11:06 pm

IN-VITRO DIAGNOSTIC REAGENT SET

Page Type
Cleared 510(K)
510(k) Number
K930074
510(k) Type
Traditional
Applicant
HORIZON DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
124 days
Submission Type
Statement

IN-VITRO DIAGNOSTIC REAGENT SET

Page Type
Cleared 510(K)
510(k) Number
K930074
510(k) Type
Traditional
Applicant
HORIZON DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
124 days
Submission Type
Statement