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

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE

K Number: K884043 · Decision Nov 16, 1988
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
15
Review Days
51

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Basic Information

Device Name
GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE
K Number
K884043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Grieshaber & Co.
Date Received
September 26, 1988
Decision Date
November 16, 1988
Product Code
HQE
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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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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