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FDA 510(k) Applications Submitted by SHERYL RUPPEL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970353
01/30/1997
AURA TEK FDP
PERIMMUNE, INC.
K991074
03/31/1999
BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST
INTRACEL CORP.
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