FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CEDARS-SINAI QUANTITIVE THALLIUM 201 ANALYSIS

K Number: K932701 · Decision Mar 29, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
12
Review Days
299

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Basic Information

Device Name
CEDARS-SINAI QUANTITIVE THALLIUM 201 ANALYSIS
K Number
K932701
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuccardiac Software, Inc.
Date Received
June 3, 1993
Decision Date
March 29, 1994
Product Code
IYX
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
IYX Camera, Scintillation (Gamma)

Similar 510(k) Clearances

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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
K942363 CEQUAL-QUANTITATIVE 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. →