meddevicedb.com FDA Device Reference

TRU-TOUCH POWDER FREE

K905503 Class I Traditional
Decision Date
1991-01-28
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K905503
Product Code LYZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1991-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRU-TOUCH POWDER FREE received FDA 510(k) clearance under submission number K905503, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1991-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code LYZ and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.