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

GREEN-LINE BIPOLAR COAGULATION UNIT

K Number: K860479 · Decision May 1, 1986
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
83

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Basic Information

Device Name
GREEN-LINE BIPOLAR COAGULATION UNIT
K Number
K860479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Grieshaber & Co.
Date Received
February 7, 1986
Decision Date
May 1, 1986
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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K914588 GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE
K914587 GRIESHABER AIR/FLUID TUBING SET
K914585 GRIESHABER TWO FUNCTION MANIPULATOR
K914586 GRIESHABER THREE FUNCTION MANIPULATOR
K897119 GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
K900714 ZZIPP INSTANT BOVIE CLEANER
K890782 GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)
K890783 GRIESHABER VISCOELASTIC INJECTION SYSTEM
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