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TR-USB TELEPHONIC STETHOSCOPE

K081032 Class II Traditional
Decision Date
2008-06-06
Sponsor / Applicant
Rnk Products, Inc.

Technical Specification

510(k) Submission ID K081032
Product Code DQD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1875
Decision Date 2008-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TR-USB TELEPHONIC STETHOSCOPE received FDA 510(k) clearance under submission number K081032, sponsored by Rnk Products, 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 2008-06-06.

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.