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

GRIESHABER VISCOELASTIC INJECTION SYSTEM

K Number: K890783 · Decision May 16, 1989
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
15
Review Days
90

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Basic Information

Device Name
GRIESHABER VISCOELASTIC INJECTION SYSTEM
K Number
K890783
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Grieshaber & Co.
Date Received
February 15, 1989
Decision Date
May 16, 1989
Product Code
FRN
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRN Pump, Infusion

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Other Clearances by Grieshaber & Co.

K Number Device Name
K950056 THE GRIESHABER AXIAL CUTTER
K930842 THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
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)
K884043 GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE
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