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

AMBLYOPIA TRAINER

K Number: K800112 · Decision Mar 10, 1980
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
6
Applicant Total
19
Review Days
54

Basic Information

Device Name
AMBLYOPIA TRAINER
K Number
K800112
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1290
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
LIFE-TECH INSTRUMENTS, INC.
Date Received
January 16, 1980
Decision Date
March 10, 1980
Product Code
HPL
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
HPL Device, Fixation, Ac-Powered, Ophthalmic

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