AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE
K-Number: K923433 · 1993-07-22
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Device Summary
Frequently Asked Questions
What is the AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE?
AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Instrumentarium Corp.. The 510(k) number is K923433.
When did AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE receive FDA 510(k) clearance?
AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE received FDA 510(k) clearance on 1993-07-22, under 510(k) number K923433.
Who is the listed applicant for AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE?
The FDA 510(k) record lists Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE?
The FDA product code for AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE is CBQ.
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 Instrumentarium Corp. 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: CBQ)
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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