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

VIT CUTTER MODEL 94

K Number: K940746 · Decision Jun 6, 1994
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
5
Review Days
108

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Basic Information

Device Name
VIT CUTTER MODEL 94
K Number
K940746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Visioncare Devices, Inc.
Date Received
February 18, 1994
Decision Date
June 6, 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

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K904909 I/A VITROPHAGE MODEL YPR 2001