S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK
K-Number: K024191 · 2003-07-02
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Device Summary
Frequently Asked Questions
What is the S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK?
S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK is a medical device that received FDA 510(k) clearance on 2003-07-02. The listed applicant is Resmed, Ltd.. The 510(k) number is K024191.
When did S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK receive FDA 510(k) clearance?
S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK received FDA 510(k) clearance on 2003-07-02, under 510(k) number K024191.
Who is the listed applicant for S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK?
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 S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK?
The FDA product code for S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK 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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