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

TOMEY PROTON TONOMETER

K Number: K924760 · Decision Apr 5, 1993
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
9
Review Days
194

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Basic Information

Device Name
TOMEY PROTON TONOMETER
K Number
K924760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tomey Corporation USA
Date Received
September 23, 1992
Decision Date
April 5, 1993
Product Code
HKY
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
HKY Tonometer, Manual

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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
K945959 VIDEO VISION ANALYZER (VIVA), VRB 100
K944910 TOMEY EM-1000 SPECULAR MICROSCOPE
K921815 TOMEY PE-300 PORTABLE ERG
K912112 PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480