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FDA 510(k)

DVT-2600

K-Number: K203016 · 2020-12-05

ApplicantDaesung Maref Co., Ltd.
Decision Date2020-12-05
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DVT-2600 is a medical device manufactured by Daesung Maref Co., Ltd.. It received FDA 510(k) clearance on 2020-12-05 under approval number K203016. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVT-2600?

DVT-2600 is a medical device that received FDA 510(k) clearance on 2020-12-05. It is manufactured by Daesung Maref Co., Ltd.. The 510(k) number is K203016.

When was DVT-2600 approved by the FDA?

DVT-2600 received FDA 510(k) clearance on 2020-12-05, under approval number K203016.

What company makes DVT-2600?

DVT-2600 is manufactured by Daesung Maref Co., Ltd..

What is the FDA product code for DVT-2600?

The FDA product code for DVT-2600 is JOW.

Other Devices by Daesung Maref Co., Ltd.

K160180Intermittent Pneumatic Compression system K150980Venous Assist System K160178Lympha-Flow(LF1200) K202395SP-1000, SP-2000 K203498LX9max K203019LF900

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Related Devices (Code: JOW)

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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.

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