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FDA 510(k)

EVOLVE

K-Number: K033551 · 2003-12-16

ApplicantReliance Orthodontic Products, Inc.
Decision Date2003-12-16
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EVOLVE 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 2003-12-16 under 510(k) number K033551. 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 EVOLVE?

EVOLVE is a medical device that received FDA 510(k) clearance on 2003-12-16. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K033551.

When did EVOLVE receive FDA 510(k) clearance?

EVOLVE received FDA 510(k) clearance on 2003-12-16, under 510(k) number K033551.

Who is the listed applicant for EVOLVE?

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 EVOLVE?

The FDA product code for EVOLVE 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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