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

RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000

K Number: K972441 · Decision Sep 4, 1997
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
66

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Basic Information

Device Name
RADIOTHERAPEUTICS RF GENERATOR. MODEL #RF-2000
K Number
K972441
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Radiotherapeutics Corp.
Date Received
June 30, 1997
Decision Date
September 4, 1997
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
K012315 LEVEEN 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
K962313 MODIFIED LEVEEN NEEDLE ELECTRODE
K962386 SENSOR SHEATH TS1
K955144 RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000
Search all 12 clearances from Radiotherapeutics Corp. →