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

DPD-510 THERAPEUTIC RADIATION DOSIMETER

K Number: K925133 · Decision Jan 4, 1993
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
47
Applicant Total
7
Review Days
83

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Basic Information

Device Name
DPD-510 THERAPEUTIC RADIATION DOSIMETER
K Number
K925133
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Scanditronix, Inc.
Date Received
October 13, 1992
Decision Date
January 4, 1993
Product Code
IWB
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
IWB System, Radiation Therapy, Radionuclide

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IWB), ordered by most recent decision date.

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Other Clearances by Scanditronix, Inc.

K Number Device Name
K934303 RFA A-300
K942092 DPD-3
K914926 SCANDIPLAN - VERSION 338
K904753 DIOLASE
K900434 MM-22 MICROTRON, MM50 MICROTRON
K843366 SUPERPETT