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MYOCARDIAL PROTECTION SYSTEM

K953838 Class II Traditional
Decision Date
1996-03-06
Sponsor / Applicant
Quest Medical, Inc.

Technical Specification

510(k) Submission ID K953838
Product Code DTR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4240
Decision Date 1996-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MYOCARDIAL PROTECTION SYSTEM received FDA 510(k) clearance under submission number K953838, sponsored by Quest Medical, 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 1996-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code DTR and 21 CFR 870.4240, within the Cardiovascular review panel as a Class II device.