meddevicedb.com FDA Device Reference

WRAPPEL T

K923408 Class II Traditional
Decision Date
1993-04-08
Sponsor / Applicant
Standard Textile Co., Inc.

Technical Specification

510(k) Submission ID K923408
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1993-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WRAPPEL T received FDA 510(k) clearance under submission number K923408, sponsored by Standard Textile Co., Inc.. 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 1993-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code FRG and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.