KIE — Apparatus, High Pressure Liquid Chromatography Class I

FDA Device Classification

Classification Details

Product Code
KIE
Device Class
Class I
Regulation Number
862.2260
Submission Type
Review Panel
TX
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K964588waters corporationWATERS 515 HPLC PUMP (515)November 29, 1996
K935666perkin-elmerPERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPApril 26, 1994
K924347milliporeWATERS(TM) 996 PDADecember 11, 1992
K914841milliporeCHROMATOGRAPHY CLINICAL USE 75JQRDecember 10, 1991
K911299rohm and haasEQUIPMENT/MATERIAL DECONTAMINATING KITApril 8, 1991
K862506milliporeTHE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORJuly 29, 1986
K844947syvaEMIT ANCILLARY REAGENTSJune 28, 1985
K844949syvaSYVA SAMPLE SEALFebruary 15, 1985
K800556hewlett-packardDIFFERENTIAL REFRACTIVE INDEX DETECTORMarch 25, 1980
K800516e.i. dupont de nemours and coDUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.March 19, 1980
K800289laboratory data controlLDC SPECTROMONITOR IIIFebruary 26, 1980
K800046laboratory data controlLDC CHROMATOGRAPHY ACCESSORY MODULE BFebruary 25, 1980
K800048laboratory data controlLDC CONSTAMETRIC III HIGHT PRESS. SOL.January 29, 1980
K800047laboratory data controlLDC UVIII FIXED WAVELENGTH ULTRAVIOLETJanuary 21, 1980
K791661waters assocSYSTEM CONTROLLER 720 SERIESSeptember 24, 1979
K782175waters assocCARTRIDGE HOLDER, RCM 100February 15, 1979
K790145waters assocSOLVENT DELIVERY SYSTEMFebruary 15, 1979
K781915waters assocDATA MODULEJanuary 10, 1979
K781771hewlett-packardDETECTOR, MODEL 79875A, VARIABLEDecember 20, 1978
K781379varian assocMODEL 5000, LIQUID CHROMATOGRAPHYSeptember 14, 1978