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ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200

K001788 Class II Traditional
Decision Date
2000-11-03
Sponsor / Applicant
Erecords Enterprises

Technical Specification

510(k) Submission ID K001788
Product Code DQD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1875
Decision Date 2000-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 received FDA 510(k) clearance under submission number K001788, sponsored by Erecords Enterprises. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code DQD and 21 CFR 870.1875, within the Cardiovascular review panel as a Class II device.