ABT 4000 VENTILATOR
K-Number: K822233 · 1982-08-27
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Device Summary
Frequently Asked Questions
What is the ABT 4000 VENTILATOR?
ABT 4000 VENTILATOR is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K822233.
When did ABT 4000 VENTILATOR receive FDA 510(k) clearance?
ABT 4000 VENTILATOR received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822233.
Who is the listed applicant for ABT 4000 VENTILATOR?
The FDA 510(k) record lists Kontron Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABT 4000 VENTILATOR?
The FDA product code for ABT 4000 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 Kontron Instruments, 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: 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
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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