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GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K925909
510(k) Type
Traditional
Applicant
ALICIA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1994
Days to Decision
723 days
Submission Type
Statement

GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K925909
510(k) Type
Traditional
Applicant
ALICIA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1994
Days to Decision
723 days
Submission Type
Statement