FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

MOSFET AUTOSENSE WIRELESS

K Number: K032725 · Decision Oct 3, 2003
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
4
Review Days
30

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Basic Information

Device Name
MOSFET AUTOSENSE WIRELESS
K Number
K032725
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thomson & Nielsen Electronics, Ltd.
Date Received
September 3, 2003
Decision Date
October 3, 2003
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

Similar 510(k) Clearances

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Other Clearances by Thomson & Nielsen Electronics, Ltd.

K Number Device Name
K041557 MOBILEMOSFET WIRELESS DOSIMETRY SYSTEM, MODEL TN-RD-70-W
K013279 MOSFET AUTOSENSE, MODEL TN-RD-60
K010472 PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50