DT-703
K-Number: K221233 · 2022-06-27
ApplicantEcotron Co., Ltd.
Decision Date2022-06-27
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
DT-703 is a medical device manufactured by Ecotron Co., Ltd.. It received FDA 510(k) clearance on 2022-06-27 under approval number K221233. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DT-703?
DT-703 is a medical device that received FDA 510(k) clearance on 2022-06-27. It is manufactured by Ecotron Co., Ltd.. The 510(k) number is K221233.
When was DT-703 approved by the FDA?
DT-703 received FDA 510(k) clearance on 2022-06-27, under approval number K221233.
What company makes DT-703?
DT-703 is manufactured by Ecotron Co., Ltd..
What is the FDA product code for DT-703?
The FDA product code for DT-703 is EHD.
Other Devices by Ecotron Co., Ltd.
Related Devices (Code: EHD)
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.