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

TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM

K Number: K031831 · Decision Dec 19, 2003
Classifications
1
FEI Numbers
74
Registration Numbers
75
Same Product Code
34
Applicant Total
11
Review Days
189

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Basic Information

Device Name
TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM
K Number
K031831
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1760
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Topcon Medical Systems, Inc.
Date Received
June 13, 2003
Decision Date
December 19, 2003
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

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