LimFlow Vector— 510(k) K221902
Substantially EquivalentLimFlow, Inc.
FDA 510(k) clearance K221902 for LimFlow Vector, Substantially Equivalent on 2022-12-21. Applicant: LimFlow, Inc.. Device class: 2.
Clearance details
- Applicant
- LimFlow, Inc.
- Product code
- Code MGZ
- Device class
- Class 2
- Regulation
- 21 CFR 870.4885
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
Recent devices under product code MGZ
view allMore clearances from LimFlow, Inc.
view allRecalls naming K221902
K-number listed on FDA's recall record- Z-1218-2026 — Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K221902.
Data sourced from openFDA. This site is unofficial and independent of the FDA.