RSM 2430C
K-Number: K170930 · 2017-04-27
ApplicantDRTECH Corporation
Decision Date2017-04-27
Product CodeMUE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
RSM 2430C is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2017-04-27 under approval number K170930. 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 2430C?
RSM 2430C is a medical device that received FDA 510(k) clearance on 2017-04-27. It is manufactured by DRTECH Corporation. The 510(k) number is K170930.
When was RSM 2430C approved by the FDA?
RSM 2430C received FDA 510(k) clearance on 2017-04-27, under approval number K170930.
What company makes RSM 2430C?
RSM 2430C is manufactured by DRTECH Corporation.
What is the FDA product code for RSM 2430C?
The FDA product code for RSM 2430C 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.