L4 OXYGEN CONCENTRATOR
K-Number: K061261 · 2006-06-28
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Device Summary
Frequently Asked Questions
What is the L4 OXYGEN CONCENTRATOR?
L4 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 2006-06-28. The listed applicant is Respironics, Inc.. The 510(k) number is K061261.
When did L4 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?
L4 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 2006-06-28, under 510(k) number K061261.
Who is the listed applicant for L4 OXYGEN CONCENTRATOR?
The FDA 510(k) record lists Respironics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L4 OXYGEN CONCENTRATOR?
The FDA product code for L4 OXYGEN CONCENTRATOR is CAW.
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, 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: CAW)
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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