meddevicedb.com FDA Device Reference

OLYMPUS ANGIOSCOPY PUMP

K871422 Class II Traditional
Decision Date
1987-08-12
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K871422
Product Code DQI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1800
Decision Date 1987-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS ANGIOSCOPY PUMP received FDA 510(k) clearance under submission number K871422, sponsored by Olympus 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 1987-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code DQI and 21 CFR 870.1800, within the Cardiovascular review panel as a Class II device.