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

IMAGEFUSION

K Number: K960071 · Decision Apr 17, 1996
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
12
Review Days
103

Basic Information

Device Name
IMAGEFUSION
K Number
K960071
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RADIONICS SOFTWARE APPLICATIONS, INC.
Date Received
January 5, 1996
Decision Date
April 17, 1996
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

Similar 510(k) Clearances

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Other Clearances by RADIONICS SOFTWARE APPLICATIONS, INC.

K Number Device Name
K990326 OPTICAL TRACKING SYSTEM MICROSCOPE MODULE II, MODEL OTS MMII
K974602 OPTICAL TRACKING SYSTEM (OTS)
K972905 XPLAN-1
K964801 OPTICAL TRACKING SYSTEM (OTS)
K961844 OPERATING ARM SYSTEM (OAS) [WITH CT AND MR IMAGES]
K962155 GILL-THOMAS-COSMAN(GTC) DENTAL TRAY
K951262 OPERATING ARM SYSTEM (OAS)
K944463 CRW-1 SYSTEM
K953482 XKNIFE-3
K946252 STEREOPLAN
Search all 12 clearances from RADIONICS SOFTWARE APPLICATIONS, INC. →