meddevicedb.com FDA Device Reference

IV START TRAY

K820490 Class II Traditional
Decision Date
1982-03-16
Sponsor / Applicant
Seamless Hospital Products Co.

Technical Specification

510(k) Submission ID K820490
Product Code LRS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 1982-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV START TRAY received FDA 510(k) clearance under submission number K820490, sponsored by Seamless Hospital Products Co.. 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 1982-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code LRS and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.