IMPULSE VENTILATOR
K-Number: K840345 · 1984-02-23
Advertisement
Device Summary
Frequently Asked Questions
What is the IMPULSE VENTILATOR?
IMPULSE VENTILATOR is a medical device that received FDA 510(k) clearance on 1984-02-23. The listed applicant is Healthdyne, Inc.. The 510(k) number is K840345.
When did IMPULSE VENTILATOR receive FDA 510(k) clearance?
IMPULSE VENTILATOR received FDA 510(k) clearance on 1984-02-23, under 510(k) number K840345.
Who is the listed applicant for IMPULSE VENTILATOR?
The FDA 510(k) record lists Healthdyne, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMPULSE VENTILATOR?
The FDA product code for IMPULSE 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 Healthdyne, 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.
Advertisement