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

LABSYSTEM III EP LABORATORY W/WINDOWS PLATFORM & WINDOWS EP SOFTWARE VERSION 1.0

K Number: K031000 · Decision Jun 3, 2003
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
403
Applicant Total
566
Review Days
64

Basic Information

Device Name
LABSYSTEM III EP LABORATORY W/WINDOWS PLATFORM & WINDOWS EP SOFTWARE VERSION 1.0
K Number
K031000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
C.R. BARD, INC.
Date Received
March 31, 2003
Decision Date
June 3, 2003
Product Code
DQK
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
DQK Computer, Diagnostic, Programmable

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