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FDA 510(k)

WILLI GELLER CREATION & AV PORCELAIN

K-Number: K002041 · 2000-08-16

ApplicantJensen Industries, Inc.
Decision Date2000-08-16
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILLI GELLER CREATION & AV PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Jensen Industries, Inc.. It received FDA 510(k) clearance on 2000-08-16 under 510(k) number K002041. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLI GELLER CREATION & AV PORCELAIN?

WILLI GELLER CREATION & AV PORCELAIN is a medical device that received FDA 510(k) clearance on 2000-08-16. The listed applicant is Jensen Industries, Inc.. The 510(k) number is K002041.

When did WILLI GELLER CREATION & AV PORCELAIN receive FDA 510(k) clearance?

WILLI GELLER CREATION & AV PORCELAIN received FDA 510(k) clearance on 2000-08-16, under 510(k) number K002041.

Who is the listed applicant for WILLI GELLER CREATION & AV PORCELAIN?

The FDA 510(k) record lists Jensen Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILLI GELLER CREATION & AV PORCELAIN?

The FDA product code for WILLI GELLER CREATION & AV PORCELAIN is EIH.

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Other records listing Jensen Industries, Inc. 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.

K183408Jensen Shade Effect LiquidsK112806JENSEN ZIRCONIAK111743THE INSYNC CERAMIC SYSTEMK070114CREATION CP-ZI PORCELAINK050838THE LF-P CERAMIC SYSTEMK043201WILLI GELLER CREATION ZI PORCELAIN

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Related Devices (Code: EIH)

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.

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba DandyK260918Zolid LunarisAmann Girrbach AGK260859Rosetta SM, Rosetta SPHass Corp.

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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