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

LEVEEN ELECTRODE

K Number: K012315 · Decision Oct 11, 2001
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
80

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Basic Information

Device Name
LEVEEN ELECTRODE
K Number
K012315
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radiotherapeutics Corp.
Date Received
July 23, 2001
Decision Date
October 11, 2001
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Radiotherapeutics Corp.

K Number Device Name
K011220 LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE
K000241 RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR
K982556 LEVEEN NEEDLE ELECTRODE
K000032 LEVEEN NEEDLE ELECTRODE
K982854 MR COMPATIBLE LEVEEN NEEDLE ELECTRODE
K981672 RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR
K972441 RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000
K962313 MODIFIED LEVEEN NEEDLE ELECTRODE
K962386 SENSOR SHEATH TS1
K955144 RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000
Search all 12 clearances from Radiotherapeutics Corp. →