LTV-1000 VENTILATOR
K-Number: K032226 · 2003-10-16
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Device Summary
Frequently Asked Questions
What is the LTV-1000 VENTILATOR?
LTV-1000 VENTILATOR is a medical device that received FDA 510(k) clearance on 2003-10-16. The listed applicant is Pulmonetic Systems, Inc.. The 510(k) number is K032226.
When did LTV-1000 VENTILATOR receive FDA 510(k) clearance?
LTV-1000 VENTILATOR received FDA 510(k) clearance on 2003-10-16, under 510(k) number K032226.
Who is the listed applicant for LTV-1000 VENTILATOR?
The FDA 510(k) record lists Pulmonetic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LTV-1000 VENTILATOR?
The FDA product code for LTV-1000 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 Pulmonetic Systems, 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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