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

SCANDIPLAN - VERSION 338

K Number: K914926 · Decision May 28, 1992
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
69
Applicant Total
7
Review Days
206

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Basic Information

Device Name
SCANDIPLAN - VERSION 338
K Number
K914926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5840
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Scanditronix, Inc.
Date Received
November 4, 1991
Decision Date
May 28, 1992
Product Code
KPQ
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
KPQ System, Simulation, Radiation Therapy

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Other Clearances by Scanditronix, Inc.

K Number Device Name
K934303 RFA A-300
K942092 DPD-3
K925133 DPD-510 THERAPEUTIC RADIATION DOSIMETER
K904753 DIOLASE
K900434 MM-22 MICROTRON, MM50 MICROTRON
K843366 SUPERPETT