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FDA 510(k)

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION

K-Number: K010192 · 2001-04-02

ApplicantAntyllos Medizintechnik GmbH
Decision Date2001-04-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION is the device name listed in this FDA 510(k) record. The listed applicant is Antyllos Medizintechnik GmbH. It received FDA 510(k) clearance on 2001-04-02 under 510(k) number K010192. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION?

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION is a medical device that received FDA 510(k) clearance on 2001-04-02. The listed applicant is Antyllos Medizintechnik GmbH. The 510(k) number is K010192.

When did ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION receive FDA 510(k) clearance?

ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION received FDA 510(k) clearance on 2001-04-02, under 510(k) number K010192.

Who is the listed applicant for ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION?

The FDA 510(k) record lists Antyllos Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION?

The FDA product code for ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION is GEI.

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Official Source

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