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RESECTION ABLATOR

Page Type
Cleared 510(K)
510(k) Number
K013117
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2001
Days to Decision
72 days
Submission Type
Summary

RESECTION ABLATOR

Page Type
Cleared 510(K)
510(k) Number
K013117
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2001
Days to Decision
72 days
Submission Type
Summary