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FDA 510(k)

MICTEC ENDOSCOPES AND ACCESSORIES

K-Number: K002877 · 2001-02-05

ApplicantDufner Instrumente GmbH
Decision Date2001-02-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICTEC ENDOSCOPES AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Dufner Instrumente GmbH. It received FDA 510(k) clearance on 2001-02-05 under 510(k) number K002877. 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 MICTEC ENDOSCOPES AND ACCESSORIES?

MICTEC ENDOSCOPES AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2001-02-05. The listed applicant is Dufner Instrumente GmbH. The 510(k) number is K002877.

When did MICTEC ENDOSCOPES AND ACCESSORIES receive FDA 510(k) clearance?

MICTEC ENDOSCOPES AND ACCESSORIES received FDA 510(k) clearance on 2001-02-05, under 510(k) number K002877.

Who is the listed applicant for MICTEC ENDOSCOPES AND ACCESSORIES?

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

What is the FDA product code for MICTEC ENDOSCOPES AND ACCESSORIES?

The FDA product code for MICTEC ENDOSCOPES AND ACCESSORIES is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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