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PR3 ULTRASOUND SYSTEM

K993978 Class II Traditional
Decision Date
2000-02-10
Sponsor / Applicant
Carolina Medical, Inc.

Technical Specification

510(k) Submission ID K993978
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2000-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PR3 ULTRASOUND SYSTEM received FDA 510(k) clearance under submission number K993978, sponsored by Carolina Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.