FDA Device Intelligence
HomeATRICURE, INC. › AtriClip® FlexV® LAA Exclusion System

AtriClip® FlexV® LAA Exclusion System

ATRICURE, INC. · Model ACHV35 · UDI-DI 10840143913402

PZX Prescription
1
510(k) clearances
134
Adverse events (7 deaths)
0
Recalls
10
Facilities

Description

LAA Exclusion System, ACHV35

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.