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FDA 510(k)

LIGHT CURING BONDING AGENT

K-Number: K832061 · 1983-08-31

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1983-08-31
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT CURING 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 1983-08-31 under 510(k) number K832061. 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 LIGHT CURING BONDING AGENT?

LIGHT CURING BONDING AGENT is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K832061.

When did LIGHT CURING BONDING AGENT receive FDA 510(k) clearance?

LIGHT CURING BONDING AGENT received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832061.

Who is the listed applicant for LIGHT CURING 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 LIGHT CURING BONDING AGENT?

The FDA product code for LIGHT CURING BONDING AGENT is 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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