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FDA 510(k)

SNORING CONTROL DEVICE

K-Number: K963591 · 1998-01-09

ApplicantKenneth Hilsen
Decision Date1998-01-09
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORING CONTROL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Kenneth Hilsen. It received FDA 510(k) clearance on 1998-01-09 under 510(k) number K963591. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNORING CONTROL DEVICE?

SNORING CONTROL DEVICE is a medical device that received FDA 510(k) clearance on 1998-01-09. The listed applicant is Kenneth Hilsen. The 510(k) number is K963591.

When did SNORING CONTROL DEVICE receive FDA 510(k) clearance?

SNORING CONTROL DEVICE received FDA 510(k) clearance on 1998-01-09, under 510(k) number K963591.

Who is the listed applicant for SNORING CONTROL DEVICE?

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

What is the FDA product code for SNORING CONTROL DEVICE?

The FDA product code for SNORING CONTROL DEVICE is LRK.

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Related Devices (Code: LRK)

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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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