meddevicedb.com FDA Device Reference

Hypertension Notification Feature (HTNF)

K250507 Class II Traditional
Decision Date
2025-09-11
Sponsor / Applicant
Apple, Inc.

Technical Specification

510(k) Submission ID K250507
Product Code SFR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2380
Decision Date 2025-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hypertension Notification Feature (HTNF) received FDA 510(k) clearance under submission number K250507, sponsored by Apple, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code SFR and 21 CFR 870.2380, within the Cardiovascular review panel as a Class II device.