meddevicedb.com FDA Device Reference

SW ULTRASOUND, MODELS 331, 311, 333

K991613 Class II Traditional
Decision Date
2000-12-08
Sponsor / Applicant
Starbene

Technical Specification

510(k) Submission ID K991613
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 2000-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SW ULTRASOUND, MODELS 331, 311, 333 received FDA 510(k) clearance under submission number K991613, sponsored by Starbene. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2000-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.