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FDA 510(k)

DENTAL ANTI-SNORING DEVICE

K-Number: K874416 · 1988-10-18

ApplicantOrtho Publications, Inc.
Decision Date1988-10-18
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL ANTI-SNORING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Publications, Inc.. It received FDA 510(k) clearance on 1988-10-18 under 510(k) number K874416. 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 DENTAL ANTI-SNORING DEVICE?

DENTAL ANTI-SNORING DEVICE is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Ortho Publications, Inc.. The 510(k) number is K874416.

When did DENTAL ANTI-SNORING DEVICE receive FDA 510(k) clearance?

DENTAL ANTI-SNORING DEVICE received FDA 510(k) clearance on 1988-10-18, under 510(k) number K874416.

Who is the listed applicant for DENTAL ANTI-SNORING DEVICE?

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

What is the FDA product code for DENTAL ANTI-SNORING DEVICE?

The FDA product code for DENTAL ANTI-SNORING DEVICE is LRK.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ortho Publications, Inc. as applicant

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.

K895189ADJUSTABLE SOFT PALATE LIFTER

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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