Last synced on 14 November 2025 at 11:06 pm

HeartLight Deflectable Sheath

Page Type
Cleared 510(K)
510(k) Number
K152310
510(k) Type
Traditional
Applicant
CARDIOFOCUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2016
Days to Decision
194 days
Submission Type
Summary

HeartLight Deflectable Sheath

Page Type
Cleared 510(K)
510(k) Number
K152310
510(k) Type
Traditional
Applicant
CARDIOFOCUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2016
Days to Decision
194 days
Submission Type
Summary