DVT-2600
K-Number: K203016 · 2020-12-05
Device Summary
Frequently Asked Questions
What is the DVT-2600?
DVT-2600 is a medical device that received FDA 510(k) clearance on 2020-12-05. The listed applicant is Daesung Maref Co., Ltd.. The 510(k) number is K203016.
When did DVT-2600 receive FDA 510(k) clearance?
DVT-2600 received FDA 510(k) clearance on 2020-12-05, under 510(k) number K203016.
Who is the listed applicant for DVT-2600?
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-2600?
The FDA product code for DVT-2600 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.