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DIAGNOSTIC ULTRASOUND 105 & 110

K842539 Class II Traditional
Decision Date
1985-04-10
Sponsor / Applicant
Diagnostic Ultrasound Corp.

Technical Specification

510(k) Submission ID K842539
Product Code JOP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2880
Decision Date 1985-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAGNOSTIC ULTRASOUND 105 & 110 received FDA 510(k) clearance under submission number K842539, sponsored by Diagnostic Ultrasound Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code JOP and 21 CFR 870.2880, within the Cardiovascular review panel as a Class II device.