meddevicedb.com FDA Device Reference

INJECTION FILL TUBE

K823238 Class II Traditional
Decision Date
1982-12-30
Sponsor / Applicant
Vetrex Medical Corp.

Technical Specification

510(k) Submission ID K823238
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 1982-12-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INJECTION FILL TUBE received FDA 510(k) clearance under submission number K823238, sponsored by Vetrex Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-12-30.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.