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

MODIFIED CEDARS-SINAI QUANTI THALLIUM-201 ANALYSIS

K Number: K892397 · Decision Oct 27, 1989
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
12
Review Days
203

Basic Information

Device Name
MODIFIED CEDARS-SINAI QUANTI THALLIUM-201 ANALYSIS
K Number
K892397
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
NUCCARDIAC SOFTWARE, INC.
Date Received
April 7, 1989
Decision Date
October 27, 1989
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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