510(k) K250817
K250817 is an FDA 510(k) premarket notification submitted by Vive Health, LLC for the device "Coretech Compression System (Coretech RHB3003)". The FDA issued a decision of Substantially Equivalent on August 8, 2025. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Vive Health, LLC has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 2025
- Date Received
- March 18, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Sleeve, Limb, Compressible
- Device Class
- Class II
- Regulation Number
- 870.5800
- Review Panel
- CV
- Submission Type