meddevicedb.com FDA Device Reference

3&4 WAY PLASTIC STERILE STPCKS. PKG.

K792126 Class II Traditional
Decision Date
1980-01-16
Sponsor / Applicant
Tronomed, Inc.

Technical Specification

510(k) Submission ID K792126
Product Code FMG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1980-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3&4 WAY PLASTIC STERILE STPCKS. PKG. received FDA 510(k) clearance under submission number K792126, sponsored by Tronomed, 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 1980-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code FMG and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.