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KEELER ACU 22XT OPHTHALMIC CRYO UNIT

Page Type
Cleared 510(K)
510(k) Number
K874555
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1988
Days to Decision
86 days

KEELER ACU 22XT OPHTHALMIC CRYO UNIT

Page Type
Cleared 510(K)
510(k) Number
K874555
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1988
Days to Decision
86 days