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

CEQUAL-QUANTITATIVE ANALYSIS

K Number: K942363 · Decision Sep 16, 1994
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
470
Applicant Total
12
Review Days
122

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Basic Information

Device Name
CEQUAL-QUANTITATIVE ANALYSIS
K Number
K942363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuccardiac Software, Inc.
Date Received
May 17, 1994
Decision Date
September 16, 1994
Product Code
KPS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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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Other Clearances by Nuccardiac Software, Inc.

K Number Device Name
K972509 CEQUAL-QUANTITATIVE ANALYSIS FOR CARDIOLITE EXECUTING ON THE MEDASYS DIGITAL SYSTEMS COMPUTER
K970288 CLINICAL DIAGNOSTIC SOFTWARE
K944720 COMPUTER, DIAGNOSTIC, PRE-PROGRAMMED, SINGLE FUNCTION
K932701 CEDARS-SINAI QUANTITIVE THALLIUM 201 ANALYSIS
K922671 CEDARS SINAI QUANTITATIVE THALLIUM 201 ANALYSIS
K915644 CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALYSIS
K914296 CEQUAL(TM) QUANITATIVE ANALYSIS CARDIOLITE(R) SPEC
K905222 CEDARS-SINAI QUANTITATIVE TI-201 ANALYSIS CTQ 2.0
K900697 CEDARS-SINAI QUANTITATIVE THALLIUM-201 ANALYSIS
K892397 MODIFIED CEDARS-SINAI QUANTI THALLIUM-201 ANALYSIS
Search all 12 clearances from Nuccardiac Software, Inc. →