FDA 510(k) Applications Submitted by NOVOSCI CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K063355 11/07/2006 D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW NOVOSCI CORP.
K033270 10/10/2003 NOVOSCI READY SYSTEM, MODEL RS-200 NOVOSCI CORP.
K033328 10/16/2003 NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT NOVOSCI CORP.


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