Last synced on 14 November 2025 at 11:06 pm

HYPERION VISIQUANT ANA TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K013213
510(k) Type
Traditional
Applicant
HYPERION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2002
Days to Decision
251 days
Submission Type
Summary

HYPERION VISIQUANT ANA TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K013213
510(k) Type
Traditional
Applicant
HYPERION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2002
Days to Decision
251 days
Submission Type
Summary