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FDA 510(k)

RELIEF ACP ORAL CARE GEL

K-Number: K062176 · 2007-01-10

ApplicantDiscus Dental, Inc.
Decision Date2007-01-10
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RELIEF ACP ORAL CARE GEL is the device name listed in this FDA 510(k) record. The listed applicant is Discus Dental, Inc.. It received FDA 510(k) clearance on 2007-01-10 under 510(k) number K062176. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIEF ACP ORAL CARE GEL?

RELIEF ACP ORAL CARE GEL is a medical device that received FDA 510(k) clearance on 2007-01-10. The listed applicant is Discus Dental, Inc.. The 510(k) number is K062176.

When did RELIEF ACP ORAL CARE GEL receive FDA 510(k) clearance?

RELIEF ACP ORAL CARE GEL received FDA 510(k) clearance on 2007-01-10, under 510(k) number K062176.

Who is the listed applicant for RELIEF ACP ORAL CARE GEL?

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

What is the FDA product code for RELIEF ACP ORAL CARE GEL?

The FDA product code for RELIEF ACP ORAL CARE GEL is LBH.

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Related Devices (Code: LBH)

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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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