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FDA 510(k)

LED PRO SEAL

K-Number: K073243 · 2008-02-08

ApplicantReliance Orthodontic Products, Inc.
Decision Date2008-02-08
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LED PRO SEAL 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 2008-02-08 under 510(k) number K073243. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED PRO SEAL?

LED PRO SEAL is a medical device that received FDA 510(k) clearance on 2008-02-08. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K073243.

When did LED PRO SEAL receive FDA 510(k) clearance?

LED PRO SEAL received FDA 510(k) clearance on 2008-02-08, under 510(k) number K073243.

Who is the listed applicant for LED PRO SEAL?

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 LED PRO SEAL?

The FDA product code for LED PRO SEAL is EBD.

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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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