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Dentsleeve Pty., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K013154
MARK II/MARK III MANOMETRIC PERFUSION PUMP
October 19, 2001
K983665
MANOMETRIC ASSEMBLIES
May 17, 1999
K980946
MARK II CO2 FLUSH MANOMETRIC PERFUSION PUMP & MARK II MANOMETRIC PERFUSION PUMP
June 8, 1998