Advocate PTA Catheter— 510(k) K192907

Name: FDA 510(k) clearance K192907
Creator: U.S. Food and Drug Administration
Published: 2019-11-26

Substantially Equivalent

Merit Medical Systems, Inc.

FDA 510(k) clearance K192907 for Advocate PTA Catheter, Substantially Equivalent on 2019-11-26. Applicant: Merit Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Merit Medical Systems, Inc.
Product code: Code LIT
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2019-10-15
Decision date: 2019-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIT

view all

K260304 — WAVE PTA Balloon Catheter2026-05-20
K252512 — Armada 14 NC PTA Catheter2026-02-13
K251915 — Amethyst HP PTA OTW 0.035 Catheter2025-12-18
K250706 — Passeo-35 Xeo Peripheral Dilatation Catheter +5 more2025-04-04
K243704 — Parafleet SC 014 PTA Balloon Dilatation Catheter +2 more2025-02-27

More clearances from Merit Medical Systems, Inc.

view all

K261310 — FlexTract Deflectable-Rotational Dilator Sheath Set2026-07-27
K262086 — PreludeSYNC Radial Compression Device2026-07-22
K254073 — StatSeal Disc2026-05-13
K251802 — STAR RF Ablation System2026-02-13
K252892 — SCOUT MD Surgical Guidance System2025-12-19

Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.