FDA 510(k)

DUCERAGOLD, DUCERATIN

K-Number: K931808 · 1993-11-03

Decision Date1993-11-03

Product CodeELL

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DUCERAGOLD, DUCERATIN is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1993-11-03 under 510(k) number K931808. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUCERAGOLD, DUCERATIN?

DUCERAGOLD, DUCERATIN is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Degussa AG. The 510(k) number is K931808.

When did DUCERAGOLD, DUCERATIN receive FDA 510(k) clearance?

DUCERAGOLD, DUCERATIN received FDA 510(k) clearance on 1993-11-03, under 510(k) number K931808.

Who is the listed applicant for DUCERAGOLD, DUCERATIN?

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

What is the FDA product code for DUCERAGOLD, DUCERATIN?

The FDA product code for DUCERAGOLD, DUCERATIN is ELL.

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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.