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FDA 510(k)

IMPROVED SEQUENCE LIGHT CURE ADHESIVE

K-Number: K921385 · 1992-04-21

ApplicantOrmco Corp.
Decision Date1992-04-21
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPROVED 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 1992-04-21 under 510(k) number K921385. 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 IMPROVED SEQUENCE LIGHT CURE ADHESIVE?

IMPROVED SEQUENCE LIGHT CURE ADHESIVE is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Ormco Corp.. The 510(k) number is K921385.

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

IMPROVED SEQUENCE LIGHT CURE ADHESIVE received FDA 510(k) clearance on 1992-04-21, under 510(k) number K921385.

Who is the listed applicant for IMPROVED 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 IMPROVED SEQUENCE LIGHT CURE ADHESIVE?

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

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Related Devices (Code: DYH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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