KardiFlex NC Coronary Dilatation Catheter— 510(k) K202578

Name: FDA 510(k) clearance K202578
Creator: U.S. Food and Drug Administration
Published: 2021-05-06

Substantially Equivalent

Medcaptain Life Science Co., Ltd.

FDA 510(k) clearance K202578 for KardiFlex NC Coronary Dilatation Catheter, Substantially Equivalent on 2021-05-06. Applicant: Medcaptain Life Science Co., Ltd.. Device class: 2.

Clearance details

Applicant: Medcaptain Life Science Co., Ltd.
Product code: Code LOX
Device class: Class 2
Regulation: 21 CFR 870.5100
Advisory panel: Cardiovascular
Date received: 2020-09-08
Decision date: 2021-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LOX

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K261428 — NC Euphora Rapid Exchange Balloon Dilatation Catheter2026-08-14
K261759 — Euphora Rapid Exchange (RX) Balloon Dilatation Catheter2026-07-27
K252116 — Firefighter Pro PTCA Balloon Catheter2026-04-07
K254022 — FLASH Flex Aorto-Ostial Angioplasty System2026-04-02
K252295 — Ryurei2026-03-27

More clearances from Medcaptain Life Science Co., Ltd.

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K230528 — Extension Set2023-12-01
K213004 — Needle Free Connector2022-05-10
K202619 — KardiFlex PTCA Balloon Dilatation Catheter2021-04-29
K202748 — Enteral Feeding Catheter2021-04-09

Adverse events under product code LOX

product code LOX

Death: 190
Injury: 1,498
Malfunction: 9,670
Total: 11,358

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.