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AUDICOR COR SENSOR (AND ACCESSORY ADAPTOR)

K030316 Class II Traditional
Decision Date
2003-08-07
Sponsor / Applicant
Inovise Medical, Inc.

Technical Specification

510(k) Submission ID K030316
Product Code DRX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2360
Decision Date 2003-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUDICOR COR SENSOR (AND ACCESSORY ADAPTOR) received FDA 510(k) clearance under submission number K030316, sponsored by Inovise Medical, 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 2003-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.