meddevicedb.com FDA Device Reference

F&P Nova Nasal Mask

K243583 Class II Traditional
Decision Date
2025-06-18
Sponsor / Applicant
Fisher & Paykel Healthcare Limited

Technical Specification

510(k) Submission ID K243583
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2025-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

F&P Nova Nasal Mask received FDA 510(k) clearance under submission number K243583, sponsored by Fisher & Paykel Healthcare Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2025-06-18.

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.