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HEART TECHNOLOGY ROTABLATOR WIRECLIP

Page Type
Cleared 510(K)
510(k) Number
K913450
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1991
Days to Decision
35 days
Submission Type
Statement

HEART TECHNOLOGY ROTABLATOR WIRECLIP

Page Type
Cleared 510(K)
510(k) Number
K913450
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1991
Days to Decision
35 days
Submission Type
Statement