510(k) K191107
K191107 is an FDA 510(k) premarket notification submitted by Alleva Medical (D.G), Ltd. for the device "Plexus". The FDA issued a decision of Substantially Equivalent on Aug 27, 2019. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 27, 2019
- Date Received
- Apr 26, 2019
- 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)