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FDA 510(k)

THE TONGUE BRUSH

K-Number: K901408 · 1990-05-21

ApplicantGarry Laboratories, Inc.
Decision Date1990-05-21
Product CodeLCN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE TONGUE BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Garry Laboratories, Inc.. It received FDA 510(k) clearance on 1990-05-21 under 510(k) number K901408. The device is classified under product code LCN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TONGUE BRUSH?

THE TONGUE BRUSH is a medical device that received FDA 510(k) clearance on 1990-05-21. The listed applicant is Garry Laboratories, Inc.. The 510(k) number is K901408.

When did THE TONGUE BRUSH receive FDA 510(k) clearance?

THE TONGUE BRUSH received FDA 510(k) clearance on 1990-05-21, under 510(k) number K901408.

Who is the listed applicant for THE TONGUE BRUSH?

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

What is the FDA product code for THE TONGUE BRUSH?

The FDA product code for THE TONGUE BRUSH is LCN.

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Related Devices (Code: LCN)

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.

K992270MIRACLEBREATH TONGUE CLEANERStellar Labs, Inc.K990344ORALGIENE TONGUE CLEANEROralgiene USA, Inc.K983683UNIK TONGUE CLEANERUnik Products, Inc.K983087BREATHTIQUE TONGUE SCRAPERCustom Medical Arts, Inc.K981808BREATHAID TONGUE SCRAPERBreathaid, LLCK980842COPPER TONGUE SCRAPEROntel Products Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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