Last synced on 14 November 2025 at 11:06 pm

ACCUFRAME

Page Type
Cleared 510(K)
510(k) Number
K081157
510(k) Type
Traditional
Applicant
CAGENIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2008
Days to Decision
90 days
Submission Type
Summary

ACCUFRAME

Page Type
Cleared 510(K)
510(k) Number
K081157
510(k) Type
Traditional
Applicant
CAGENIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2008
Days to Decision
90 days
Submission Type
Summary