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RESECTION ABLATOR

Page Type
Cleared 510(K)
510(k) Number
K013369
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2002
Days to Decision
175 days
Submission Type
Summary

RESECTION ABLATOR

Page Type
Cleared 510(K)
510(k) Number
K013369
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2002
Days to Decision
175 days
Submission Type
Summary