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FDA 510(k)

RESTRAXX DATA CENTRE, MODEL R10

K-Number: K070746 · 2007-07-13

ApplicantResmed, Ltd.
Decision Date2007-07-13
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESTRAXX DATA CENTRE, MODEL R10 is the device name listed in this FDA 510(k) record. The listed applicant is Resmed, Ltd.. It received FDA 510(k) clearance on 2007-07-13 under 510(k) number K070746. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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