EasyCare Tx 2
K-Number: K241939 · 2024-09-27
Device Summary
Frequently Asked Questions
What is the EasyCare Tx 2?
EasyCare Tx 2 is a medical device that received FDA 510(k) clearance on 2024-09-27. The listed applicant is Resmed Corp. The 510(k) number is K241939.
When did EasyCare Tx 2 receive FDA 510(k) clearance?
EasyCare Tx 2 received FDA 510(k) clearance on 2024-09-27, under 510(k) number K241939.
Who is the listed applicant for EasyCare Tx 2?
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 EasyCare Tx 2?
The FDA product code for EasyCare Tx 2 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.