DT-703
K-Number: K221233 · 2022-06-27
Device Summary
Frequently Asked Questions
What is the DT-703?
DT-703 is a medical device that received FDA 510(k) clearance on 2022-06-27. The listed applicant is Ecotron Co., Ltd.. The 510(k) number is K221233.
When did DT-703 receive FDA 510(k) clearance?
DT-703 received FDA 510(k) clearance on 2022-06-27, under 510(k) number K221233.
Who is the listed applicant for DT-703?
The FDA 510(k) record lists Ecotron Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DT-703?
The FDA product code for DT-703 is EHD.
Other records listing Ecotron Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EHD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.