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FDA 510(k)

MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55

K-Number: K042434 · 2004-11-03

ApplicantNOUVAG AG
Decision Date2004-11-03
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 is the device name listed in this FDA 510(k) record. The listed applicant is NOUVAG AG. It received FDA 510(k) clearance on 2004-11-03 under 510(k) number K042434. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55?

MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 is a medical device that received FDA 510(k) clearance on 2004-11-03. The listed applicant is NOUVAG AG. The 510(k) number is K042434.

When did MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 receive FDA 510(k) clearance?

MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 received FDA 510(k) clearance on 2004-11-03, under 510(k) number K042434.

Who is the listed applicant for MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55?

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

What is the FDA product code for MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55?

The FDA product code for MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 is DZI.

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Official Source

View on FDA Database →

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

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