meddevicedb.com FDA Device Reference

ANGIOGRAPHY KIT

K821976 Class II Traditional
Decision Date
1982-07-20
Sponsor / Applicant
Mallinckrodt Critical Care

Technical Specification

510(k) Submission ID K821976
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1982-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANGIOGRAPHY KIT received FDA 510(k) clearance under submission number K821976, sponsored by Mallinckrodt Critical Care. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.