RSM 1824C with RConsole1
K-Number: K162670 · 2017-02-23
ApplicantDRTECH Corporation
Decision Date2017-02-23
Product CodeMUE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RSM 1824C with RConsole1 is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2017-02-23 under approval number K162670. The device is classified under product code MUE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RSM 1824C with RConsole1?
RSM 1824C with RConsole1 is a medical device that received FDA 510(k) clearance on 2017-02-23. It is manufactured by DRTECH Corporation. The 510(k) number is K162670.
When was RSM 1824C with RConsole1 approved by the FDA?
RSM 1824C with RConsole1 received FDA 510(k) clearance on 2017-02-23, under approval number K162670.
What company makes RSM 1824C with RConsole1?
RSM 1824C with RConsole1 is manufactured by DRTECH Corporation.
What is the FDA product code for RSM 1824C with RConsole1?
The FDA product code for RSM 1824C with RConsole1 is MUE.
Other Devices by DRTECH Corporation
Related Devices (Code: MUE)
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.