EASYCARE TX SYSTEM (CONNEXUNS)
K-Number: K113780 · 2012-04-20
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Device Summary
Frequently Asked Questions
What is the EASYCARE TX SYSTEM (CONNEXUNS)?
EASYCARE TX SYSTEM (CONNEXUNS) is a medical device that received FDA 510(k) clearance on 2012-04-20. The listed applicant is Resmed, Ltd.. The 510(k) number is K113780.
When did EASYCARE TX SYSTEM (CONNEXUNS) receive FDA 510(k) clearance?
EASYCARE TX SYSTEM (CONNEXUNS) received FDA 510(k) clearance on 2012-04-20, under 510(k) number K113780.
Who is the listed applicant for EASYCARE TX SYSTEM (CONNEXUNS)?
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 EASYCARE TX SYSTEM (CONNEXUNS)?
The FDA product code for EASYCARE TX SYSTEM (CONNEXUNS) 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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