meddevicedb.com FDA Device Reference

Cardinal Health™ Poly Reinforced Surgical Gown

K253243 Class II Abbreviated
Decision Date
2026-04-28
Sponsor / Applicant
Cardinal Health 200, LLC

Technical Specification

510(k) Submission ID K253243
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2026-04-28
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cardinal Health™ Poly Reinforced Surgical Gown received FDA 510(k) clearance under submission number K253243, sponsored by Cardinal Health 200, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-04-28.

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.