meddevicedb.com FDA Device Reference

3.5 & 5.5 OZ. SODIUM CHLORIDE SOLUTION

K820460 Class II Traditional
Decision Date
1982-03-08
Sponsor / Applicant
Superior Plastic Products Corp.

Technical Specification

510(k) Submission ID K820460
Product Code JOL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1982-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3.5 & 5.5 OZ. SODIUM CHLORIDE SOLUTION received FDA 510(k) clearance under submission number K820460, sponsored by Superior Plastic Products Corp.. 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 1982-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code JOL and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.