SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System
K-Number: K203310 · 2021-04-02
Decision Date2021-04-02
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System is a medical device manufactured by Jiangsu Synecoun Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-04-02 under approval number K203310. 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 SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System?
SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System is a medical device that received FDA 510(k) clearance on 2021-04-02. It is manufactured by Jiangsu Synecoun Medical Technology Co., Ltd.. The 510(k) number is K203310.
When was SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System approved by the FDA?
SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System received FDA 510(k) clearance on 2021-04-02, under approval number K203310.
What company makes SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System?
SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System is manufactured by Jiangsu Synecoun Medical Technology Co., Ltd..
What is the FDA product code for SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System?
The FDA product code for SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System is 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.