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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