DVT-4000S
K-Number: K203417 · 2021-03-28
Device Summary
Frequently Asked Questions
What is the DVT-4000S?
DVT-4000S is a medical device that received FDA 510(k) clearance on 2021-03-28. The listed applicant is Daesung Maref Co., Ltd.. The 510(k) number is K203417.
When did DVT-4000S receive FDA 510(k) clearance?
DVT-4000S received FDA 510(k) clearance on 2021-03-28, under 510(k) number K203417.
Who is the listed applicant for DVT-4000S?
The FDA 510(k) record lists Daesung Maref Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DVT-4000S?
The FDA product code for DVT-4000S is JOW.
Other records listing Daesung Maref 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: JOW)
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.