HP PTA Balloon Dilatation Catheter— 510(k) K231402

Name: FDA 510(k) clearance K231402
Creator: U.S. Food and Drug Administration
Published: 2023-12-20

Substantially Equivalent

Kossel Medtech (Suzhou) Co., Ltd.

FDA 510(k) clearance K231402 for HP PTA Balloon Dilatation Catheter, Substantially Equivalent on 2023-12-20. Applicant: Kossel Medtech (Suzhou) Co., Ltd.. Device class: 2.

Clearance details

Applicant: Kossel Medtech (Suzhou) Co., Ltd.
Product code: Code LIT
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2023-05-15
Decision date: 2023-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suzhou, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIT

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K254212 — NC PTA Balloon Dilatation Catheter2026-09-16
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

More clearances from Kossel Medtech (Suzhou) Co., Ltd.

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K221245 — PTA Balloon Dilatation Catheter2022-12-14
K211349 — Selebrek PTCA Balloon Dilatation Catheter2022-01-07
K211393 — Selethru(TM) NC PTCA Balloon Dilatation Catheter2021-07-02
K182699 — Selethru PTCA Balloon Dilatation Catheter2018-11-26

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.