meddevicedb.com FDA Device Reference

Personalized Therapy Comfort Settings (PTCS)

K251657 Class II Traditional
Decision Date
2025-12-05
Sponsor / Applicant
Resmed Corp

Technical Specification

510(k) Submission ID K251657
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2025-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Personalized Therapy Comfort Settings (PTCS) received FDA 510(k) clearance under submission number K251657, sponsored by Resmed Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2025-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.