510(k) K200083
K200083 is an FDA 510(k) premarket notification submitted by Embolic Acceleration, LLC for the device "EMBA Hourglass Peripheral Embolization Device (PED)". The FDA issued a decision of Substantially Equivalent on Feb 14, 2020. The device falls under product code KRD (Device, Vascular, For Promoting Embolization), a Class II device regulated under 21 CFR 870.3300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 14, 2020
- Date Received
- Jan 15, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Vascular, For Promoting Embolization
- Device Class
- Class II
- Regulation Number
- 870.3300
- Review Panel
- CV
- Submission Type
- 510(k)