meddevicedb.com FDA Device Reference

JEHLE CORONARY PERFUSION CATHETERS

K874242 Class II Traditional
Decision Date
1987-12-07
Sponsor / Applicant
Pilling Co.

Technical Specification

510(k) Submission ID K874242
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 1987-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JEHLE CORONARY PERFUSION CATHETERS received FDA 510(k) clearance under submission number K874242, sponsored by Pilling Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1987-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.