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MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT

K843934 Class II Traditional
Decision Date
1984-11-20
Sponsor / Applicant
Future Impex Corp.

Technical Specification

510(k) Submission ID K843934
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1984-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT received FDA 510(k) clearance under submission number K843934, sponsored by Future Impex 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 1984-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.