FDA 510(k) Applications Submitted by PAT AMTOWER

FDA 510(k) Number Submission Date Device Name Applicant
K990311 02/01/1999 VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER ABX DIAGNOSTICS
K991839 05/28/1999 ABX PENTRA 120 RETIC AUTOMATED HEMATOLOGY ANALYZER ABX DIAGNOSTICS
K992511 07/27/1999 ABX PENTRA 60 HEMATOLOGY ANALYZER ABX DIAGNOSTICS


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