Last synced on 14 November 2025 at 11:06 pm

EDWARD PROPLEGE PERIPHERAL RETROGRADE CARDIOPLEGIA DEVICE

Page Type
Cleared 510(K)
510(k) Number
K120780
510(k) Type
Traditional
Applicant
EDWARDS LIFESCIENCES, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2012
Days to Decision
105 days
Submission Type
Summary

EDWARD PROPLEGE PERIPHERAL RETROGRADE CARDIOPLEGIA DEVICE

Page Type
Cleared 510(K)
510(k) Number
K120780
510(k) Type
Traditional
Applicant
EDWARDS LIFESCIENCES, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2012
Days to Decision
105 days
Submission Type
Summary