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ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010192
510(k) Type
Traditional
Applicant
ANTYLLOS MEDIZINTECHNIK GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/2/2001
Days to Decision
70 days
Submission Type
Summary

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010192
510(k) Type
Traditional
Applicant
ANTYLLOS MEDIZINTECHNIK GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/2/2001
Days to Decision
70 days
Submission Type
Summary