meddevicedb.com FDA Device Reference

ABCOM 2000

K912562 Class II Traditional
Decision Date
1992-01-09
Sponsor / Applicant
Applied Biometrics, Inc.

Technical Specification

510(k) Submission ID K912562
Product Code DPW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2100
Decision Date 1992-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABCOM 2000 received FDA 510(k) clearance under submission number K912562, sponsored by Applied Biometrics, 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 1992-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code DPW and 21 CFR 870.2100, within the Cardiovascular review panel as a Class II device.