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FDA 510(k)

ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM

K-Number: K871295 · 1987-05-29

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1987-05-29
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM 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 1987-05-29 under 510(k) number K871295. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM?

ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K871295.

When did ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM receive FDA 510(k) clearance?

ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871295.

Who is the listed applicant for ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM?

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 ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM?

The FDA product code for ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM is EBF.

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Related Devices (Code: EBF)

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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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