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CONTRAST MEDIA INJECT. SET CMS

K833645 Class II Traditional
Decision Date
1984-04-17
Sponsor / Applicant
Gish Biomedical, Inc.

Technical Specification

510(k) Submission ID K833645
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 1984-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTRAST MEDIA INJECT. SET CMS received FDA 510(k) clearance under submission number K833645, sponsored by Gish Biomedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-04-17.

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.