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HICUT HIGHSPEED INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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