RESTRAXX DATA CENTRE, MODEL R10
K-Number: K070746 · 2007-07-13
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Device Summary
Frequently Asked Questions
What is the RESTRAXX DATA CENTRE, MODEL R10?
RESTRAXX DATA CENTRE, MODEL R10 is a medical device that received FDA 510(k) clearance on 2007-07-13. The listed applicant is Resmed, Ltd.. The 510(k) number is K070746.
When did RESTRAXX DATA CENTRE, MODEL R10 receive FDA 510(k) clearance?
RESTRAXX DATA CENTRE, MODEL R10 received FDA 510(k) clearance on 2007-07-13, under 510(k) number K070746.
Who is the listed applicant for RESTRAXX DATA CENTRE, MODEL R10?
The FDA 510(k) record lists Resmed, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESTRAXX DATA CENTRE, MODEL R10?
The FDA product code for RESTRAXX DATA CENTRE, MODEL R10 is BZD.
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 Resmed, Ltd. 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: BZD)
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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