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CRYOPHTHALMIC UNIT

Page Type
Cleared 510(K)
510(k) Number
K811244
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1981
Days to Decision
50 days

CRYOPHTHALMIC UNIT

Page Type
Cleared 510(K)
510(k) Number
K811244
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1981
Days to Decision
50 days