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

STELLARTECH COAGULATION SYSTEM

K Number: K013139 · Decision Dec 18, 2001
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
11
Review Days
90

Basic Information

Device Name
STELLARTECH COAGULATION SYSTEM
K Number
K013139
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
STELLARTECH RESEARCH CORP.
Date Received
September 19, 2001
Decision Date
December 18, 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 STELLARTECH RESEARCH CORP.

K Number Device Name
K061544 STELLARTECH 100 COAGULATION SYSTEM
K050831 STELLARTECH COAGULATION SYSTEM 2, MODELS 1100C-115A AND 1100C-230A
K042909 STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230A
K041383 STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 AND 1100C-230
K040240 STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
K032721 MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
K032452 MODIFICATION TO: STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 & 100C-230
K032062 STELLARTECH COAGULATION SYSTEM, MODELS (1100C-115 & 1100C-230)
K023765 STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
K994173 STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230
Search all 11 clearances from STELLARTECH RESEARCH CORP. →