AS/3 COMPACT AIRWAY MODULE M-CAIOV
K-Number: K960490 · 1996-05-03
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Device Summary
Frequently Asked Questions
What is the AS/3 COMPACT AIRWAY MODULE M-CAIOV?
AS/3 COMPACT AIRWAY MODULE M-CAIOV is a medical device that received FDA 510(k) clearance on 1996-05-03. The listed applicant is Datex Medical Instrumentation, Inc.. The 510(k) number is K960490.
When did AS/3 COMPACT AIRWAY MODULE M-CAIOV receive FDA 510(k) clearance?
AS/3 COMPACT AIRWAY MODULE M-CAIOV received FDA 510(k) clearance on 1996-05-03, under 510(k) number K960490.
Who is the listed applicant for AS/3 COMPACT AIRWAY MODULE M-CAIOV?
The FDA 510(k) record lists Datex Medical Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AS/3 COMPACT AIRWAY MODULE M-CAIOV?
The FDA product code for AS/3 COMPACT AIRWAY MODULE M-CAIOV is CBS.
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 Datex Medical Instrumentation, 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: CBS)
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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