meddevicedb.com FDA Device Reference

Digistat Care

K261287 Class II Traditional
Decision Date
2026-09-12
Sponsor / Applicant
Ascom Ums Srl Unipersonale

Technical Specification

510(k) Submission ID K261287
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2026-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Digistat Care received FDA 510(k) clearance under submission number K261287, sponsored by Ascom Ums Srl Unipersonale. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.