meddevicedb.com FDA Device Reference

NYES Tuff Cuff L3 Disposable Gowns

K261949 Class II Special
Decision Date
2026-07-10
Sponsor / Applicant
New York Embroidery Studio

Technical Specification

510(k) Submission ID K261949
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2026-07-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NYES Tuff Cuff L3 Disposable Gowns received FDA 510(k) clearance under submission number K261949, sponsored by New York Embroidery Studio. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-07-10.

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.