meddevicedb.com FDA Device Reference

PACE-PULSE/COMPUTRAC

K800782 Class II Traditional
Decision Date
1980-05-28
Sponsor / Applicant
Bib, Inc.

Technical Specification

510(k) Submission ID K800782
Product Code KRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3640
Decision Date 1980-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACE-PULSE/COMPUTRAC received FDA 510(k) clearance under submission number K800782, sponsored by Bib, 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 1980-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code KRE and 21 CFR 870.3640, within the Cardiovascular review panel as a Class II device.