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GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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