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FDA 510(k)

SNOREMASTER SNORE REMEDY

K-Number: K932932 · 1995-02-10

ApplicantThe Snoremaster Co.
Decision Date1995-02-10
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNOREMASTER SNORE REMEDY is the device name listed in this FDA 510(k) record. The listed applicant is The Snoremaster Co.. It received FDA 510(k) clearance on 1995-02-10 under 510(k) number K932932. 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 SNOREMASTER SNORE REMEDY?

SNOREMASTER SNORE REMEDY is a medical device that received FDA 510(k) clearance on 1995-02-10. The listed applicant is The Snoremaster Co.. The 510(k) number is K932932.

When did SNOREMASTER SNORE REMEDY receive FDA 510(k) clearance?

SNOREMASTER SNORE REMEDY received FDA 510(k) clearance on 1995-02-10, under 510(k) number K932932.

Who is the listed applicant for SNOREMASTER SNORE REMEDY?

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

What is the FDA product code for SNOREMASTER SNORE REMEDY?

The FDA product code for SNOREMASTER SNORE REMEDY is LQZ.

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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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