FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

NICOM

K Number: K042144 · Decision Nov 12, 2004
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
7
Review Days
95

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Basic Information

Device Name
NICOM
K Number
K042144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cheetah Medical, Inc.
Date Received
August 9, 2004
Decision Date
November 12, 2004
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

Similar 510(k) Clearances

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Other Clearances by Cheetah Medical, Inc.

K Number Device Name
K103166 CHEETAH RELIANT
K101487 CHEETAH NICOM SYSTEM
K083093 CHEETAH RELIANT
K071631 NICOM ELECTRODES
K072662 CHEETAH RELIANT, CHEETAH ACTIVE
K023370 CHEETAH I.V.D.S., MODEL 2002P