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FDA 510(k)

DE LUXE

K-Number: K925755 · 1993-12-03

ApplicantRudolf Riester GmbH & Co. KG
Decision Date1993-12-03
Product CodeHLJ
Advisory CommitteeOP
DecisionUnknown

Device Summary

DE LUXE is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Riester GmbH & Co. KG. It received FDA 510(k) clearance on 1993-12-03 under 510(k) number K925755. The device is classified under product code HLJ. It was reviewed by the OP advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DE LUXE?

DE LUXE is a medical device that received FDA 510(k) clearance on 1993-12-03. The listed applicant is Rudolf Riester GmbH & Co. KG. The 510(k) number is K925755.

When did DE LUXE receive FDA 510(k) clearance?

DE LUXE received FDA 510(k) clearance on 1993-12-03, under 510(k) number K925755.

Who is the listed applicant for DE LUXE?

The FDA 510(k) record lists Rudolf Riester GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DE LUXE?

The FDA product code for DE LUXE is HLJ.

Other records listing Rudolf Riester GmbH & Co. KG as applicant

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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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