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CPE 2000 CARDIO PULMONARY ERGOMETER

K874925 Class I Traditional
Decision Date
1988-01-19
Sponsor / Applicant
Medical Graphics Corp.

Technical Specification

510(k) Submission ID K874925
Product Code KRI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4200
Decision Date 1988-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CPE 2000 CARDIO PULMONARY ERGOMETER received FDA 510(k) clearance under submission number K874925, sponsored by Medical Graphics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code KRI and 21 CFR 870.4200, within the Cardiovascular review panel as a Class I device.