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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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