meddevicedb.com FDA Device Reference

Dream Medi Sterile Surgical Gown (SurgicalGownUL)

K242937 Class II Traditional
Decision Date
2025-05-05
Sponsor / Applicant
Dae Myung Chemical Co., Ltd. (Vietnam)

Technical Specification

510(k) Submission ID K242937
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2025-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dream Medi Sterile Surgical Gown (SurgicalGownUL) received FDA 510(k) clearance under submission number K242937, sponsored by Dae Myung Chemical Co., Ltd. (Vietnam). 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 2025-05-05.

Classification & Regulation

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