meddevicedb.com FDA Device Reference

BARD BIOPOTENTIAL AMPLIFIER

K874441 Class II Traditional
Decision Date
1988-01-19
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K874441
Product Code DRR
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2050
Decision Date 1988-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARD BIOPOTENTIAL AMPLIFIER received FDA 510(k) clearance under submission number K874441, sponsored by C.R. Bard, 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 1988-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code DRR and 21 CFR 870.2050, within the Cardiovascular review panel as a Class II device.