EConsole1
K-Number: K231225 · 2023-10-18
ApplicantDRTECH Corporation
Decision Date2023-10-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EConsole1 is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2023-10-18 under approval number K231225. 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 EConsole1?
EConsole1 is a medical device that received FDA 510(k) clearance on 2023-10-18. It is manufactured by DRTECH Corporation. The 510(k) number is K231225.
When was EConsole1 approved by the FDA?
EConsole1 received FDA 510(k) clearance on 2023-10-18, under approval number K231225.
What company makes EConsole1?
EConsole1 is manufactured by DRTECH Corporation.
What is the FDA product code for EConsole1?
The FDA product code for EConsole1 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.