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PreludeSYNC™ Radial Compression Device

K262086 Class II Special
Decision Date
2026-07-22
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K262086
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2026-07-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PreludeSYNC™ Radial Compression Device received FDA 510(k) clearance under submission number K262086, sponsored by Merit Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.