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HEART CATHETERIZATION TRAY

K860161 Class II Traditional
Decision Date
1986-05-02
Sponsor / Applicant
Medical Design Concepts, Inc.

Technical Specification

510(k) Submission ID K860161
Product Code DRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1310
Decision Date 1986-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEART CATHETERIZATION TRAY received FDA 510(k) clearance under submission number K860161, sponsored by Medical Design Concepts, 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 1986-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.