EConsole2
K-Number: K240243 · 2024-09-23
ApplicantDRTECH Corporation
Decision Date2024-09-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EConsole2 is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2024-09-23 under approval number K240243. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EConsole2?
EConsole2 is a medical device that received FDA 510(k) clearance on 2024-09-23. It is manufactured by DRTECH Corporation. The 510(k) number is K240243.
When was EConsole2 approved by the FDA?
EConsole2 received FDA 510(k) clearance on 2024-09-23, under approval number K240243.
What company makes EConsole2?
EConsole2 is manufactured by DRTECH Corporation.
What is the FDA product code for EConsole2?
The FDA product code for EConsole2 is LLZ.
Other Devices by DRTECH Corporation
Related Devices (Code: LLZ)
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.