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

DPD-3

K Number: K942092 · Decision Jul 29, 1994
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
7
Review Days
88

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Basic Information

Device Name
DPD-3
K Number
K942092
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scanditronix, Inc.
Date Received
May 2, 1994
Decision Date
July 29, 1994
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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K Number Device Name
K934303 RFA A-300
K925133 DPD-510 THERAPEUTIC RADIATION DOSIMETER
K914926 SCANDIPLAN - VERSION 338
K904753 DIOLASE
K900434 MM-22 MICROTRON, MM50 MICROTRON
K843366 SUPERPETT