PHOENIX ANESTHESIA MACHINE
K-Number: K853139 · 1985-08-26
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Device Summary
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
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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