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LQ1106 OPHTHALMIC YAG LASER

Page Type
Cleared 510(K)
510(k) Number
K882772
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1988
Days to Decision
51 days

LQ1106 OPHTHALMIC YAG LASER

Page Type
Cleared 510(K)
510(k) Number
K882772
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1988
Days to Decision
51 days