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

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE

K Number: K930842 · Decision May 3, 1994
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
148
Applicant Total
15
Review Days
440

Basic Information

Device Name
THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
K Number
K930842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GRIESHABER & CO.
Date Received
February 17, 1993
Decision Date
May 3, 1994
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

Similar 510(k) Clearances

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

View all

Other Clearances by GRIESHABER & CO.

K Number Device Name
K950056 THE GRIESHABER AXIAL CUTTER
K914588 GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE
K914587 GRIESHABER AIR/FLUID TUBING SET
K914586 GRIESHABER THREE FUNCTION MANIPULATOR
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
Search all 15 clearances from GRIESHABER & CO. →