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FDA 510(k)

AS/3 COMPACT AIRWAY MODULE M-CAIOV

K-Number: K960490 · 1996-05-03

Decision Date1996-05-03
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AS/3 COMPACT AIRWAY MODULE M-CAIOV is the device name listed in this FDA 510(k) record. The listed applicant is Datex Medical Instrumentation, Inc.. It received FDA 510(k) clearance on 1996-05-03 under 510(k) number K960490. The device is classified under product code CBS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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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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