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FDA 510(k)

ET-3 EMERGENCY TRANSPORT VENTILATOR

K-Number: K823861 · 1983-02-07

Decision Date1983-02-07
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ET-3 EMERGENCY TRANSPORT VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Med Devices, Inc.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K823861. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ET-3 EMERGENCY TRANSPORT VENTILATOR?

ET-3 EMERGENCY TRANSPORT VENTILATOR is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Bio-Med Devices, Inc.. The 510(k) number is K823861.

When did ET-3 EMERGENCY TRANSPORT VENTILATOR receive FDA 510(k) clearance?

ET-3 EMERGENCY TRANSPORT VENTILATOR received FDA 510(k) clearance on 1983-02-07, under 510(k) number K823861.

Who is the listed applicant for ET-3 EMERGENCY TRANSPORT VENTILATOR?

The FDA 510(k) record lists Bio-Med Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ET-3 EMERGENCY TRANSPORT VENTILATOR?

The FDA product code for ET-3 EMERGENCY TRANSPORT VENTILATOR is CBK.

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 Bio-Med Devices, 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.

View all 14 devices →

Related Devices (Code: CBK)

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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