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FDA 510(k)

YRNSORTIP OXIMANOMETER

K-Number: K093981 · 2010-07-22

ApplicantCnoga Medical , Ltd.
Decision Date2010-07-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

YRNSORTIP OXIMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Cnoga Medical , Ltd.. It received FDA 510(k) clearance on 2010-07-22 under 510(k) number K093981. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YRNSORTIP OXIMANOMETER?

YRNSORTIP OXIMANOMETER is a medical device that received FDA 510(k) clearance on 2010-07-22. The listed applicant is Cnoga Medical , Ltd.. The 510(k) number is K093981.

When did YRNSORTIP OXIMANOMETER receive FDA 510(k) clearance?

YRNSORTIP OXIMANOMETER received FDA 510(k) clearance on 2010-07-22, under 510(k) number K093981.

Who is the listed applicant for YRNSORTIP OXIMANOMETER?

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

What is the FDA product code for YRNSORTIP OXIMANOMETER?

The FDA product code for YRNSORTIP OXIMANOMETER is DXN.

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Related Devices (Code: DXN)

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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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