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FDA 510(k)

KWIKKMODEL

K-Number: K001414 · 2000-08-09

ApplicantR-Dental Dentalerzeugnisse GmbH
Decision Date2000-08-09
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KWIKKMODEL is the device name listed in this FDA 510(k) record. The listed applicant is R-Dental Dentalerzeugnisse GmbH. It received FDA 510(k) clearance on 2000-08-09 under 510(k) number K001414. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KWIKKMODEL?

KWIKKMODEL is a medical device that received FDA 510(k) clearance on 2000-08-09. The listed applicant is R-Dental Dentalerzeugnisse GmbH. The 510(k) number is K001414.

When did KWIKKMODEL receive FDA 510(k) clearance?

KWIKKMODEL received FDA 510(k) clearance on 2000-08-09, under 510(k) number K001414.

Who is the listed applicant for KWIKKMODEL?

The FDA 510(k) record lists R-Dental Dentalerzeugnisse GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KWIKKMODEL?

The FDA product code for KWIKKMODEL is ELW.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing R-Dental Dentalerzeugnisse GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K010926R-SI-LINE METAL-BITE

Related Devices (Code: ELW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254152Dia-X Sil Light BodyDiaDent Group InternationalK254142Dia-X Sil Heavy BodyDiaDent Group InternationalK254112Dia-X Sil BiteDiaDent Group InternationalK253501Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set - 454g (1lb) (052327); Chroma Print Premium Fast Set - 454g (1lb) (052457); Chroma Print Premium Regular Set - 454g (1lb) (051460); Perfil Pro - 454g (1lb) (056213); Perfil Pro+ - 454g (1lb) (056121); Perfil Pro Chroma - 454g (1lb) (056122); Hydro Print Premium Fast Set - Multi Pack (056205); Hydro Print Premium Regular Set - Multi Pack (056208); Hydro Print Premium Fast Set - 9,07Kg (20lb) (056204);Vigodent Indústria E Comercio LtdaK250969JET BITE; JET BLUE BITE FAST; JET BLUE BITE SUPERFASTDent4you AGK241924Elastic Impression MaterialBeijing Okvd Biological Technology , Ltd.

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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