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

MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA

K Number: K000073 · Decision Mar 1, 2000
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
15
Review Days
51

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Basic Information

Device Name
MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
K Number
K000073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mercury Medical
Date Received
January 10, 2000
Decision Date
March 1, 2000
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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