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

STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)

K Number: K023765 · Decision Nov 29, 2002
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
17

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Basic Information

Device Name
STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
K Number
K023765
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stellartech Research Corp.
Date Received
November 12, 2002
Decision Date
November 29, 2002
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

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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)
K013139 STELLARTECH COAGULATION SYSTEM
K994173 STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230
Search all 11 clearances from Stellartech Research Corp. →