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FDA 510(k)

ULTIMA SNORING MIKE, MODEL 0540

K-Number: K020312 · 2002-08-07

ApplicantBraebon Medical Corp.
Decision Date2002-08-07
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTIMA SNORING MIKE, MODEL 0540 is the device name listed in this FDA 510(k) record. The listed applicant is Braebon Medical Corp.. It received FDA 510(k) clearance on 2002-08-07 under 510(k) number K020312. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMA SNORING MIKE, MODEL 0540?

ULTIMA SNORING MIKE, MODEL 0540 is a medical device that received FDA 510(k) clearance on 2002-08-07. The listed applicant is Braebon Medical Corp.. The 510(k) number is K020312.

When did ULTIMA SNORING MIKE, MODEL 0540 receive FDA 510(k) clearance?

ULTIMA SNORING MIKE, MODEL 0540 received FDA 510(k) clearance on 2002-08-07, under 510(k) number K020312.

Who is the listed applicant for ULTIMA SNORING MIKE, MODEL 0540?

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

What is the FDA product code for ULTIMA SNORING MIKE, MODEL 0540?

The FDA product code for ULTIMA SNORING MIKE, MODEL 0540 is MNR.

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Other records listing Braebon Medical Corp. as applicant

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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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