Last synced on 14 November 2025 at 11:06 pm

AMBLYOPIA TRAINER

Page Type
Cleared 510(K)
510(k) Number
K800112
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1980
Days to Decision
54 days

AMBLYOPIA TRAINER

Page Type
Cleared 510(K)
510(k) Number
K800112
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1980
Days to Decision
54 days