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

SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF

K Number: K013255 · Decision Nov 7, 2001
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
40

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Basic Information

Device Name
SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF
K Number
K013255
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
Ellman Intl., Inc.
Date Received
September 28, 2001
Decision Date
November 7, 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 Ellman Intl., Inc.

K Number Device Name
K003126 BIPOLAR TRIGGER-FLEX PROBE
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K001253 SURGITRON IEC II
K992382 SURGITRON RADIOLASE
K990146 SURGITRON
K980177 SUGITRON MODEL: IEC
K980170 SURGITRON
K972072 SURGITRON MODEL FFPF-EMC
K955176 DENTO-SURGE
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