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FDA 510(k)

SNORENTI

K-Number: K032410 · 2005-02-28

ApplicantJames P Boyd
Decision Date2005-02-28
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORENTI is the device name listed in this FDA 510(k) record. The listed applicant is James P Boyd. It received FDA 510(k) clearance on 2005-02-28 under 510(k) number K032410. 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 SNORENTI?

SNORENTI is a medical device that received FDA 510(k) clearance on 2005-02-28. The listed applicant is James P Boyd. The 510(k) number is K032410.

When did SNORENTI receive FDA 510(k) clearance?

SNORENTI received FDA 510(k) clearance on 2005-02-28, under 510(k) number K032410.

Who is the listed applicant for SNORENTI?

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

What is the FDA product code for SNORENTI?

The FDA product code for SNORENTI 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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