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FDA 510(k)

PHOENIX ANESTHESIA MACHINE

K-Number: K853139 · 1985-08-26

Decision Date1985-08-26
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHOENIX ANESTHESIA MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is American Anesthesia, Inc.. It received FDA 510(k) clearance on 1985-08-26 under 510(k) number K853139. 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 PHOENIX ANESTHESIA MACHINE?

PHOENIX ANESTHESIA MACHINE is a medical device that received FDA 510(k) clearance on 1985-08-26. The listed applicant is American Anesthesia, Inc.. The 510(k) number is K853139.

When did PHOENIX ANESTHESIA MACHINE receive FDA 510(k) clearance?

PHOENIX ANESTHESIA MACHINE received FDA 510(k) clearance on 1985-08-26, under 510(k) number K853139.

Who is the listed applicant for PHOENIX ANESTHESIA MACHINE?

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

What is the FDA product code for PHOENIX ANESTHESIA MACHINE?

The FDA product code for PHOENIX 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 American Anesthesia, 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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