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FDA 510(k)

BREATH TAKER

K-Number: K971887 · 1997-06-10

ApplicantHofa, LLC
Decision Date1997-06-10
Product CodeLCN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BREATH TAKER is the device name listed in this FDA 510(k) record. The listed applicant is Hofa, LLC. It received FDA 510(k) clearance on 1997-06-10 under 510(k) number K971887. 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 BREATH TAKER?

BREATH TAKER is a medical device that received FDA 510(k) clearance on 1997-06-10. The listed applicant is Hofa, LLC. The 510(k) number is K971887.

When did BREATH TAKER receive FDA 510(k) clearance?

BREATH TAKER received FDA 510(k) clearance on 1997-06-10, under 510(k) number K971887.

Who is the listed applicant for BREATH TAKER?

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

What is the FDA product code for BREATH TAKER?

The FDA product code for BREATH TAKER is LCN.

Related Clinical Trials

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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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