Millipore Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
30
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSJanuary 17, 2003
K013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RApril 4, 2002
K963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)June 10, 1997
K941326ULTRAFREE-CLMay 27, 1994
K934069MILLEX, DUALEX (PLUS, ULTRA)April 21, 1994
K924347WATERS(TM) 996 PDADecember 11, 1992
K922388WATERS(TM) LC MODULE I FOR CLINICAL USESeptember 11, 1992
K920136WATERS 717 AUTOSAMPLERFebruary 19, 1992
K914841CHROMATOGRAPHY CLINICAL USE 75JQRDecember 10, 1991
K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETESeptember 11, 1990
K872792WATERS M600E MULTI-SOLVENT DELIVERY SYSTEMJuly 31, 1987
K872582HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEMJuly 16, 1987
K870949WATERS 650 ADVANCED PROTEIN PURIFICATION SYSTEMApril 22, 1987
K864267SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)January 9, 1987
K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORJuly 29, 1986
K850272WATERS 740 DATA MODULE-PLOTTER INTEGRATORMarch 6, 1985
K850359WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL DMarch 5, 1985
K841403HEMO-RO WATER PURIFICATION SYSJuly 6, 1984
K832952MILLIPORE IVEX INT FILTER UNITOctober 4, 1983
K811432MILLIPORE DUAL RATE INTRAVENOUS CASSETTEJuly 13, 1981