FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

LEKSELL GAMMAPLAN 4C WITH MULTIVIEW

K Number: K042269 · Decision Sep 8, 2004
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
35
Review Days
16

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Basic Information

Device Name
LEKSELL GAMMAPLAN 4C WITH MULTIVIEW
K Number
K042269
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elekta Instrument AB
Date Received
August 23, 2004
Decision Date
September 8, 2004
Product Code
MUJ
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
MUJ System, Planning, Radiation Therapy Treatment

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Other Clearances by Elekta Instrument AB

K Number Device Name
K190887 Leksell Vantage Stereotactic System
K173789 Leksell Gamma Knife Perfexion, Leksell Gamma Knife Icon
K173791 Leksell GammaPlan
K171123 Leksell Vantage Stereotactic System
K160440 Leksell Gamma Knife Icon
K152558 Leksell Stereotactic System, Injection/ Aspiration Needle Kit
K151159 Leksell Gamma Knife Perfexion
K151666 Leksell GammaPlan
K151561 Leksell Gamma Knife Icon
K133565 LEKSELL GAMMA KNIFE PERFEXION
Search all 35 clearances from Elekta Instrument AB →