meddevicedb.com FDA Device Reference

E-Z PREP(R) TRAY WITH HIBICLENS(R)

K935483 Class II Traditional
Decision Date
1994-02-09
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K935483
Product Code LRO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1994-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-Z PREP(R) TRAY WITH HIBICLENS(R) received FDA 510(k) clearance under submission number K935483, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1994-02-09.

Classification & Regulation

This clearance is catalogued under FDA product code LRO and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.