meddevicedb.com FDA Device Reference

AES STOCKINGS

K822446 Class II Traditional
Decision Date
1982-08-27
Sponsor / Applicant
Rampon Products

Technical Specification

510(k) Submission ID K822446
Product Code DWL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5780
Decision Date 1982-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AES STOCKINGS received FDA 510(k) clearance under submission number K822446, sponsored by Rampon Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1982-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code DWL and 21 CFR 880.5780, within the General Hospital review panel as a Class II device.