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

VAXIOM FAMILY OF RF LESION PROBES & ELEC

K Number: K802243 · Decision Nov 12, 1980
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
17
Review Days
57

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Basic Information

Device Name
VAXIOM FAMILY OF RF LESION PROBES & ELEC
K Number
K802243
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Progress Mankind Technology
Date Received
September 16, 1980
Decision Date
November 12, 1980
Product Code
GXI
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXI Probe, Radiofrequency Lesion

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K834047 PMT-HALO/ORTHOPEDIC JACKET SYSTEM
K831329 PMT VAXIOM STEREOTACTIC SYS #FX001
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