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FDA 510(k)

MALLARD MODEL 3000 ANESTHESIA MACHINE

K-Number: K033026 · 2004-09-03

Decision Date2004-09-03
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MALLARD MODEL 3000 ANESTHESIA MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Mallard Medical, Inc.. It received FDA 510(k) clearance on 2004-09-03 under 510(k) number K033026. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALLARD MODEL 3000 ANESTHESIA MACHINE?

MALLARD MODEL 3000 ANESTHESIA MACHINE is a medical device that received FDA 510(k) clearance on 2004-09-03. The listed applicant is Mallard Medical, Inc.. The 510(k) number is K033026.

When did MALLARD MODEL 3000 ANESTHESIA MACHINE receive FDA 510(k) clearance?

MALLARD MODEL 3000 ANESTHESIA MACHINE received FDA 510(k) clearance on 2004-09-03, under 510(k) number K033026.

Who is the listed applicant for MALLARD MODEL 3000 ANESTHESIA MACHINE?

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

What is the FDA product code for MALLARD MODEL 3000 ANESTHESIA MACHINE?

The FDA product code for MALLARD MODEL 3000 ANESTHESIA MACHINE is BSZ.

Related Clinical Trials

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.

Other records listing Mallard Medical, Inc. as applicant

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.

Related Devices (Code: BSZ)

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.

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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