510(k) K203803
K203803 is an FDA 510(k) premarket notification submitted by Vasoinnovations, Inc. for the device "VASOBand Vascular Compression Device". The FDA issued a decision of Substantially Equivalent on January 26, 2021. The device falls under product code DXC (Clamp, Vascular), a Class II device regulated under 21 CFR 870.4450. Vasoinnovations, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 26, 2021
- Date Received
- December 28, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Clamp, Vascular
- Device Class
- Class II
- Regulation Number
- 870.4450
- Review Panel
- CV
- Submission Type