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LARIAT II SUTURE DELIVERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090385
510(k) Type
Traditional
Applicant
SENTREHEART INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2009
Days to Decision
78 days
Submission Type
Summary

LARIAT II SUTURE DELIVERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090385
510(k) Type
Traditional
Applicant
SENTREHEART INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2009
Days to Decision
78 days
Submission Type
Summary