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

EMORY CARDIAC TOOLBOX VERSION 2.6

K Number: K040141 · Decision Jan 30, 2004
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
459
Applicant Total
12
Review Days
8

Basic Information

Device Name
EMORY CARDIAC TOOLBOX VERSION 2.6
K Number
K040141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYNTERMED, INC.
Date Received
January 22, 2004
Decision Date
January 30, 2004
Product Code
KPS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

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

Product Code Device Name
KPS System, Tomography, Computed, Emission

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K Number Device Name
K130902 EMORY CARDIAC TOOLBOX 3.2
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K123646 EMORY CARDIAC TOOLBOX 4.0
K072307 QUANTITATIVE NEUROQ 3.0
K071503 SYSTEM, TOMOGRAPHY, COMPUTED EMISSION
K070089 SYNTERMED LIVE
K042258 BP-SPECT V1.O
K041022 NEUROQ - PET DP
K020300 NORTHWESTERN GATED BLOOD POOL SPECT (NUMUGAS)
K014033 EMORY CARDIAC TOOLBOX 2.1 EXECUTING ON NUCLEAR MEDICINE COMPUTERS
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