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FDA 510(k)

CERESTORE DENTIN PORCELAIN

K-Number: K850821 · 1985-04-08

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-04-08
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERESTORE DENTIN PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1985-04-08 under 510(k) number K850821. 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 CERESTORE DENTIN PORCELAIN?

CERESTORE DENTIN PORCELAIN is a medical device that received FDA 510(k) clearance on 1985-04-08. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K850821.

When did CERESTORE DENTIN PORCELAIN receive FDA 510(k) clearance?

CERESTORE DENTIN PORCELAIN received FDA 510(k) clearance on 1985-04-08, under 510(k) number K850821.

Who is the listed applicant for CERESTORE DENTIN PORCELAIN?

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

What is the FDA product code for CERESTORE DENTIN PORCELAIN?

The FDA product code for CERESTORE DENTIN PORCELAIN is EIH.

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Related Devices (Code: EIH)

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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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