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LARIAT sulture Delivery Device

Page Type
Cleared 510(K)
510(k) Number
K142241
510(k) Type
Special
Applicant
SENTREHEART INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2014
Days to Decision
30 days
Submission Type
Summary

LARIAT sulture Delivery Device

Page Type
Cleared 510(K)
510(k) Number
K142241
510(k) Type
Special
Applicant
SENTREHEART INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2014
Days to Decision
30 days
Submission Type
Summary