FDA 510(k) Applications Submitted by LEROY J FISCHBACH

FDA 510(k) Number Submission Date Device Name Applicant
K962707 07/12/1996 MINNTECH MINNIFILTER PLUS HEMOFILTER AND TUBING SET MINNTECH CORP.
K960513 02/05/1996 PERACT 20 LIQUID STERILANT MINNTECH CORP.
K953821 08/15/1995 BIOCOR 200 HARDSHELL VENOUS RESERVIOR MINNTECH CORP.


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