FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NOVA MICROSONICS DATAVUE ECHO ANALYSIS SYSTEM

K Number: K897004 · Decision Mar 13, 1990
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
61
Review Days
85

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Basic Information

Device Name
NOVA MICROSONICS DATAVUE ECHO ANALYSIS SYSTEM
K Number
K897004
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Advanced Technology Laboratories, Inc.
Date Received
December 18, 1989
Decision Date
March 13, 1990
Product Code
DXG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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