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

ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM

K Number: K993923 · Decision Apr 7, 2000
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
88
Review Days
141

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Basic Information

Device Name
ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM
K Number
K993923
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Adac Laboratories
Date Received
November 18, 1999
Decision Date
April 7, 2000
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 Adac Laboratories

K Number Device Name
K062298 APOLLO GAMMA CAMERA SYSTEM
K061029 JETSTREAM WORKSPACE
K060020 AUTOQUANT PLUS
K051351 PRECEDENCE SPECT/CT IMAGING SYSTEM
K042880 JETSTREAM WORKSPACE
K042903 AUTOSPECS
K041577 PINNACLE3 RADIATION THERAPY PLANNING SYSTEM
K041218 GRIFFIN SPECT/CT IMAGING SYSTEM
K041182 SYNTEGRA
K040326 AUTOQUANT PLUS
Search all 88 clearances from Adac Laboratories →