FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GRIESHABER THREE FUNCTION MANIPULATOR

K Number: K914586 · Decision Jan 3, 1992
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
48
Applicant Total
15
Review Days
79

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Basic Information

Device Name
GRIESHABER THREE FUNCTION MANIPULATOR
K Number
K914586
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4350
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Grieshaber & Co.
Date Received
October 16, 1991
Decision Date
January 3, 1992
Product Code
EQH
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EQH Source, Carrier, Fiberoptic Light

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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
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
K884043 GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE
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