FDA 510(k) Applications Submitted by LON BRUSO

FDA 510(k) Number Submission Date Device Name Applicant
K990246 01/26/1999 STERI-PAK LF BOWIE-DICK TEST PACK STERITEC PRODUCTS MFG. CO., INC.
K982188 06/22/1998 STERI-PAK BOWIE DICK TEST PACK STERITEC PRODUCTS MFG. CO., INC.


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