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FDA 510(k)

IST SNORING APPLIANCE

K-Number: K090911 · 2009-09-11

ApplicantDental Crafters
Decision Date2009-09-11
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IST SNORING APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Dental Crafters. It received FDA 510(k) clearance on 2009-09-11 under 510(k) number K090911. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IST SNORING APPLIANCE?

IST SNORING APPLIANCE is a medical device that received FDA 510(k) clearance on 2009-09-11. The listed applicant is Dental Crafters. The 510(k) number is K090911.

When did IST SNORING APPLIANCE receive FDA 510(k) clearance?

IST SNORING APPLIANCE received FDA 510(k) clearance on 2009-09-11, under 510(k) number K090911.

Who is the listed applicant for IST SNORING APPLIANCE?

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

What is the FDA product code for IST SNORING APPLIANCE?

The FDA product code for IST SNORING APPLIANCE is LQZ.

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Related Devices (Code: LQZ)

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.

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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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