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

ORTHOCAD SOFTWARE OPTION

K Number: K120288 · Decision Sep 19, 2012
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
24
Review Days
232

Basic Information

Device Name
ORTHOCAD SOFTWARE OPTION
K Number
K120288
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ESAOTE, S.P.A.
Date Received
January 31, 2012
Decision Date
September 19, 2012
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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Other Clearances by ESAOTE, S.P.A.

K Number Device Name
K142421 G-scan Brio
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K131996 S-SCAN
K132231 MYLABSEVEN, MYLABALPHA
K122006 G-SCAN BRIO
K121650 S-SCAN
K121384 MYLABSOGNO
K120748 SPEEDUP SOFTWARE OPTION
K111302 MYLABSEVEN, MYLABALPHA
K111803 G-SCAN
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