meddevicedb.com FDA Device Reference

PERCOR 9.5 FR IAB ON DATASCOPE CO2

K833828 Class II Traditional
Decision Date
1985-02-08
Sponsor / Applicant
Datascope Corp.

Technical Specification

510(k) Submission ID K833828
Product Code DSP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3535
Decision Date 1985-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERCOR 9.5 FR IAB ON DATASCOPE CO2 received FDA 510(k) clearance under submission number K833828, sponsored by Datascope 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 1985-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code DSP and 21 CFR 870.3535, within the Cardiovascular review panel as a Class II device.