meddevicedb.com FDA Device Reference

PRIMED Surgical Masks and PRIMED Procedure Masks

K240286 Class II Traditional
Decision Date
2024-08-26
Sponsor / Applicant
Primed Medical Products, Inc.

Technical Specification

510(k) Submission ID K240286
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2024-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIMED Surgical Masks and PRIMED Procedure Masks received FDA 510(k) clearance under submission number K240286, sponsored by Primed Medical Products, Inc.. 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 2024-08-26.

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.