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FDA 510(k)

PRAXAIR MEDICAL AIR MIXER

K-Number: K051192 · 2005-09-06

ApplicantPraxair, Inc.
Decision Date2005-09-06
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRAXAIR MEDICAL AIR MIXER is the device name listed in this FDA 510(k) record. The listed applicant is Praxair, Inc.. It received FDA 510(k) clearance on 2005-09-06 under 510(k) number K051192. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRAXAIR MEDICAL AIR MIXER?

PRAXAIR MEDICAL AIR MIXER is a medical device that received FDA 510(k) clearance on 2005-09-06. The listed applicant is Praxair, Inc.. The 510(k) number is K051192.

When did PRAXAIR MEDICAL AIR MIXER receive FDA 510(k) clearance?

PRAXAIR MEDICAL AIR MIXER received FDA 510(k) clearance on 2005-09-06, under 510(k) number K051192.

Who is the listed applicant for PRAXAIR MEDICAL AIR MIXER?

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

What is the FDA product code for PRAXAIR MEDICAL AIR MIXER?

The FDA product code for PRAXAIR MEDICAL AIR MIXER is BZR.

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Other records listing Praxair, Inc. as applicant

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Related Devices (Code: BZR)

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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