meddevicedb.com FDA Device Reference

PRIMED AAMI Level 3 Open Back Gowns

K262007 Class II Traditional
Decision Date
2026-09-11
Sponsor / Applicant
PRIMED Medical Products, Inc.

Technical Specification

510(k) Submission ID K262007
Product Code QPC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2026-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIMED AAMI Level 3 Open Back Gowns received FDA 510(k) clearance under submission number K262007, 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 2026-09-11.

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.