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VIVAWAVE MICROWAVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053535
510(k) Type
Traditional
Applicant
VALLEYLAB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2006
Days to Decision
129 days
Submission Type
Summary

VIVAWAVE MICROWAVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053535
510(k) Type
Traditional
Applicant
VALLEYLAB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2006
Days to Decision
129 days
Submission Type
Summary