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

EMPRINT PROCEDURE PLANNING APPLICATION

K Number: K142048 · Decision Sep 17, 2014
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
44
Review Days
51

Basic Information

Device Name
EMPRINT PROCEDURE PLANNING APPLICATION
K Number
K142048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien LLC
Date Received
July 28, 2014
Decision Date
September 17, 2014
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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