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FDA 510(k)

SEQUENCE LIGHT CURE ADHESIVE

K-Number: K914727 · 1992-01-17

ApplicantOrmco Corp.
Decision Date1992-01-17
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SEQUENCE LIGHT CURE ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Ormco Corp.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K914727. 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 SEQUENCE LIGHT CURE ADHESIVE?

SEQUENCE LIGHT CURE ADHESIVE is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Ormco Corp.. The 510(k) number is K914727.

When did SEQUENCE LIGHT CURE ADHESIVE receive FDA 510(k) clearance?

SEQUENCE LIGHT CURE ADHESIVE received FDA 510(k) clearance on 1992-01-17, under 510(k) number K914727.

Who is the listed applicant for SEQUENCE LIGHT CURE ADHESIVE?

The FDA 510(k) record lists Ormco Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEQUENCE LIGHT CURE ADHESIVE?

The FDA product code for SEQUENCE LIGHT CURE ADHESIVE is DYH.

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Related Devices (Code: 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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