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

NIDEK MODEL VST-4000

K Number: K924353 · Decision Mar 29, 1993
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
77
Review Days
213

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Basic Information

Device Name
NIDEK MODEL VST-4000
K Number
K924353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nidek, Inc.
Date Received
August 28, 1992
Decision Date
March 29, 1993
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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K Number Device Name
K050336 OPD-STATION SOFTWARE
K042785 MULTI COLOR LASER PHOTOCOAGULATOR, MODEL MC-300
K031733 NON-CONTACT TONOMETER, MODEL NT-4000
K032085 GREEN LASER PHOTOCOAGULATOR MODEL GYC-1000
K013694 NIDEK ADVANCED VISION INFORMATION SYSTEM (NAVIS)
K020876 ECHOSCAN, MODEL US-1800
K014274 NON-MYDRIATIC FUNDUS CAMERA, MODEL NM-1000
K013760 DC-3300 LASER DIODE PHOTOCOAGULATOR
K013864 MODIFICATION TO EPI-STAR SURGICAL LASER SYSTEM, M0DEL DS-60
K990119 EPI-STAR SURGICAL LASER SYSTER
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