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FDA 510(k) Applications Submitted by INTRACEL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990664
03/01/1999
PRIMA SYSTEM - OLD, BARTELS ELISA - NEW
INTRACEL CORP.
K982311
07/01/1998
BARTELS CINAKIT CMV ANTIGENEMIA
INTRACEL CORP.
K003204
10/13/2000
BARTELS VIRAL RESPIRATORY SCREENING AND IDENTIFICATION KIT
INTRACEL CORP.
K991074
03/31/1999
BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST
INTRACEL CORP.
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