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FDA 510(k)

EXCEL REGULAR SET

K-Number: K875141 · 1988-02-26

ApplicantReliance Orthodontic Products, Inc.
Decision Date1988-02-26
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EXCEL REGULAR SET is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Orthodontic Products, Inc.. It received FDA 510(k) clearance on 1988-02-26 under 510(k) number K875141. 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 EXCEL REGULAR SET?

EXCEL REGULAR SET is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K875141.

When did EXCEL REGULAR SET receive FDA 510(k) clearance?

EXCEL REGULAR SET received FDA 510(k) clearance on 1988-02-26, under 510(k) number K875141.

Who is the listed applicant for EXCEL REGULAR SET?

The FDA 510(k) record lists Reliance Orthodontic Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXCEL REGULAR SET?

The FDA product code for EXCEL REGULAR SET 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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