510(k) K203310
K203310 is an FDA 510(k) premarket notification submitted by Jiangsu Synecoun Medical Technology Co., Ltd. for the device "SyneCare 1000 Deep Vein Thrombosis Prevention Therapy System". The FDA issued a decision of Substantially Equivalent on Apr 2, 2021. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Jiangsu Synecoun Medical Technology Co., Ltd. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 2, 2021
- Date Received
- Nov 10, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sleeve, Limb, Compressible
- Device Class
- Class II
- Regulation Number
- 870.5800
- Review Panel
- CV
- Submission Type
- 510(k)