S7 ELITE CP AP SYSTEM
K-Number: K013909 · 2002-07-08
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Device Summary
Frequently Asked Questions
What is the S7 ELITE CP AP SYSTEM?
S7 ELITE CP AP SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-08. The listed applicant is Resmed Corp. The 510(k) number is K013909.
When did S7 ELITE CP AP SYSTEM receive FDA 510(k) clearance?
S7 ELITE CP AP SYSTEM received FDA 510(k) clearance on 2002-07-08, under 510(k) number K013909.
Who is the listed applicant for S7 ELITE CP AP SYSTEM?
The FDA 510(k) record lists Resmed Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S7 ELITE CP AP SYSTEM?
The FDA product code for S7 ELITE CP AP SYSTEM 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 Corp 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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