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

SYNTERMED LIVE

K Number: K070089 · Decision Mar 2, 2007
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
12
Review Days
52

Basic Information

Device Name
SYNTERMED LIVE
K Number
K070089
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYNTERMED, INC.
Date Received
January 9, 2007
Decision Date
March 2, 2007
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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K042258 BP-SPECT V1.O
K041022 NEUROQ - PET DP
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