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FDA 510(k)

SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM

K-Number: K082528 · 2009-03-06

ApplicantNoble Anesthesia-Air, Inc.
Decision Date2009-03-06
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Noble Anesthesia-Air, Inc.. It received FDA 510(k) clearance on 2009-03-06 under 510(k) number K082528. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM?

SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 2009-03-06. The listed applicant is Noble Anesthesia-Air, Inc.. The 510(k) number is K082528.

When did SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM receive FDA 510(k) clearance?

SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM received FDA 510(k) clearance on 2009-03-06, under 510(k) number K082528.

Who is the listed applicant for SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM?

The FDA 510(k) record lists Noble Anesthesia-Air, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM?

The FDA product code for SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM is DQD.

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Related Devices (Code: DQD)

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

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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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