510(k) K904792

DIAGNOSTIC ULTRASOUND VERSADOPP 1000 by Diagnostic Ultrasound Corp. — Product Code DPW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 28, 1991
Date Received
October 23, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Flowmeter, Blood, Cardiovascular
Device Class
Class II
Regulation Number
870.2100
Review Panel
CV
Submission Type