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FDA 510(k)

J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT

K-Number: K850073 · 1985-02-08

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-02-08
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT 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 1985-02-08 under 510(k) number K850073. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT?

J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT is a medical device that received FDA 510(k) clearance on 1985-02-08. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K850073.

When did J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT receive FDA 510(k) clearance?

J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT received FDA 510(k) clearance on 1985-02-08, under 510(k) number K850073.

Who is the listed applicant for J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT?

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 J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT?

The FDA product code for J & J LIGHT CURING DENTIN/ENAMEL BONDING AGENT is EBD.

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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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