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ANCA COMBI DIAGNOSTIC KIT WITH IF-AIM TECHNOLOGY

Page Type
Cleared 510(K)
510(k) Number
K001127
510(k) Type
Traditional
Applicant
THE BINDING SITE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2000
Days to Decision
149 days
Submission Type
Statement

ANCA COMBI DIAGNOSTIC KIT WITH IF-AIM TECHNOLOGY

Page Type
Cleared 510(K)
510(k) Number
K001127
510(k) Type
Traditional
Applicant
THE BINDING SITE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2000
Days to Decision
149 days
Submission Type
Statement