meddevicedb.com FDA Device Reference

VR® Personal Protective Level 3 Gown (VR Gowns)

K252940 Class II Traditional
Decision Date
2025-12-16
Sponsor / Applicant
PolyConversions, Inc.

Technical Specification

510(k) Submission ID K252940
Product Code QPC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2025-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VR® Personal Protective Level 3 Gown (VR Gowns) received FDA 510(k) clearance under submission number K252940, sponsored by PolyConversions, 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 2025-12-16.

Classification & Regulation

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