meddevicedb.com FDA Device Reference

STERILE WATER

K933526 Class II Traditional
Decision Date
1994-03-10
Sponsor / Applicant
Trinity Laboratories, Inc.

Technical Specification

510(k) Submission ID K933526
Product Code JOL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1994-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE WATER received FDA 510(k) clearance under submission number K933526, sponsored by Trinity Laboratories, 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 1994-03-10.

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.