meddevicedb.com FDA Device Reference

EPICARDIA PC/FC

K883103 Class II Traditional
Decision Date
1988-09-22
Sponsor / Applicant
Medicomp, Inc.

Technical Specification

510(k) Submission ID K883103
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1988-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EPICARDIA PC/FC received FDA 510(k) clearance under submission number K883103, sponsored by Medicomp, 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 1988-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.