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FDA 510(k)

MERCURY VCO2

K-Number: K092217 · 2009-08-21

ApplicantRespironics Novametrix, Inc.
Decision Date2009-08-21
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY VCO2 is the device name listed in this FDA 510(k) record. The listed applicant is Respironics Novametrix, Inc.. It received FDA 510(k) clearance on 2009-08-21 under 510(k) number K092217. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCURY VCO2?

MERCURY VCO2 is a medical device that received FDA 510(k) clearance on 2009-08-21. The listed applicant is Respironics Novametrix, Inc.. The 510(k) number is K092217.

When did MERCURY VCO2 receive FDA 510(k) clearance?

MERCURY VCO2 received FDA 510(k) clearance on 2009-08-21, under 510(k) number K092217.

Who is the listed applicant for MERCURY VCO2?

The FDA 510(k) record lists Respironics Novametrix, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERCURY VCO2?

The FDA product code for MERCURY VCO2 is BZK.

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Related Devices (Code: BZK)

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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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