PLV CONTINUUM VENTILATOR, MODEL P1000
K-Number: K022750 · 2003-11-20
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Device Summary
Frequently Asked Questions
What is the PLV CONTINUUM VENTILATOR, MODEL P1000?
PLV CONTINUUM VENTILATOR, MODEL P1000 is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Respironics California, Inc.. The 510(k) number is K022750.
When did PLV CONTINUUM VENTILATOR, MODEL P1000 receive FDA 510(k) clearance?
PLV CONTINUUM VENTILATOR, MODEL P1000 received FDA 510(k) clearance on 2003-11-20, under 510(k) number K022750.
Who is the listed applicant for PLV CONTINUUM VENTILATOR, MODEL P1000?
The FDA 510(k) record lists Respironics California, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLV CONTINUUM VENTILATOR, MODEL P1000?
The FDA product code for PLV CONTINUUM VENTILATOR, MODEL P1000 is NOU.
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 Respironics California, 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: NOU)
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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