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FDA 510(k)

ACCLAIM* BRACKET ADHESIVE

K-Number: K864008 · 1986-10-24

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1986-10-24
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCLAIM* BRACKET ADHESIVE 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 1986-10-24 under 510(k) number K864008. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCLAIM* BRACKET ADHESIVE?

ACCLAIM* BRACKET ADHESIVE is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K864008.

When did ACCLAIM* BRACKET ADHESIVE receive FDA 510(k) clearance?

ACCLAIM* BRACKET ADHESIVE received FDA 510(k) clearance on 1986-10-24, under 510(k) number K864008.

Who is the listed applicant for ACCLAIM* BRACKET ADHESIVE?

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 ACCLAIM* BRACKET ADHESIVE?

The FDA product code for ACCLAIM* BRACKET ADHESIVE is DYH.

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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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