meddevicedb.com FDA Device Reference

Grande Medical Masks, Model SF-600

K232968 Class II Traditional
Decision Date
2024-06-06
Sponsor / Applicant
Golden Grande Corp.

Technical Specification

510(k) Submission ID K232968
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2024-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Grande Medical Masks, Model SF-600 received FDA 510(k) clearance under submission number K232968, sponsored by Golden Grande Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.