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HICUT HIGHSPEED INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K130755
510(k) Type
Traditional
Applicant
ADEOR MEDICAL AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/27/2014
Days to Decision
465 days
Submission Type
Summary

HICUT HIGHSPEED INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K130755
510(k) Type
Traditional
Applicant
ADEOR MEDICAL AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/27/2014
Days to Decision
465 days
Submission Type
Summary