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

VIDEO VISION ANALYZER (VIVA), VRB 100

K Number: K945959 · Decision Mar 1, 1995
Classifications
1
FEI Numbers
74
Registration Numbers
75
Same Product Code
34
Applicant Total
9
Review Days
84

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Basic Information

Device Name
VIDEO VISION ANALYZER (VIVA), VRB 100
K Number
K945959
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1760
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tomey Corporation USA
Date Received
December 7, 1994
Decision Date
March 1, 1995
Product Code
HKO
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
HKO Refractometer, Ophthalmic

Similar 510(k) Clearances

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Other Clearances by Tomey Corporation USA

K Number Device Name
K971953 CONFOSCAN
K971685 IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM
K961805 TOMEY DTL ELECTRODE
K932571 TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4
K944910 TOMEY EM-1000 SPECULAR MICROSCOPE
K924760 TOMEY PROTON TONOMETER
K921815 TOMEY PE-300 PORTABLE ERG
K912112 PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480