MMX
LimFlow V-Ceiver
- Advisory panel
- Cardiovascular
- Total cleared
- 32
Adverse events under product code MMX
product code MMX- Death
- 3
- Total
- 3
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code MMX
- K242776 — LimFlow V-Ceiver
- K241259 — Amplatz Goose Neck Snare Kit
- K232443 — Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
- K222254 — Gunther Tulip Vena Cava Filter Retrieval Set
- K222083 — LimFlow V-Ceiver
- K212988 — ONO Retrieval Device
- K213494 — Aveir Retrieval Catheter
- K200963 — Halo Single-Loop Microsnare Kit
- K200268 — Halo Single-Loop Snare Kit
- K193507 — Merit ONE Snare System
- K191758 — Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
- K181757 — Günther Tulip® Vena Cava Filter Retrieval Set
- K170987 — Captus Vascular Retrieval System
- K163307 — Expro Elite Snare, Sympro Elite Snare
- K160593 — Indy OTW Vascular Retriever
- K152136 — Recovery Cone Removal System
- K152560 — Bard Snare Retrieval Kit
- K151497 — EN Snare Endovascular Snare System
- K142265 — ONE Snare Endovascular Microsnare System
- K133681 — CRUX SNARE FILTER RETRIEVAL SET
- K122088 — MERIT ONE SNARE SYSTEM
- K112185 — FOURSNARE VASCULAR RETRIEVAL SNARE
- K102484 — SEQURE SNARE SYSTEM
- K092343 — EN SNARE ENDOVASCULAR SNARE SYSTEM
- K091563 — RECRUIT MICROCATHETER
- K071457 — MODIFICATION TO RADIUS SNARE
- K050926 — TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060
- K033188 — TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050
- K022201 — RADIUS MICRO SNARE
- K021441 — RADIUS SNARE
- K021606 — EN-SNARE ENDOVASCULAR SNARE AND CATHETER
- K014109 — IN-TIME RETRIEVAL DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.