Last synced on 14 November 2025 at 11:06 pm

LVIVO EF SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130779
510(k) Type
Traditional
Applicant
DIACARDIO, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2013
Days to Decision
147 days
Submission Type
Summary

LVIVO EF SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130779
510(k) Type
Traditional
Applicant
DIACARDIO, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2013
Days to Decision
147 days
Submission Type
Summary