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Novosci Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K072499
NOVOFLO CATHETER LT
October 30, 2007
K063355
D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW
July 27, 2007
K033270
NOVOSCI READY SYSTEM, MODEL RS-200
February 13, 2004
K033328
NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT
January 16, 2004