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510(k) K781771

Device
Detector, Model 79875a, Variable
Applicant
HEWLETT-PACKARD CO.
510(k) number
K781771
Product code
KIE
Decision
Substantially Equivalent (SESE)
Decision date
1978-12-20
Date received
1978-10-13
Regulation
862.2260
Classification name
Apparatus, High Pressure Liquid Chromatography
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KIE#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K964588WATERS 515 HPLC PUMP (515)Waters Corporation1996-11-29
K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.1994-04-26
K924347WATERS(TM) 996 PDAMillipore Corp.1992-12-11
K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.1991-12-10
K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.1991-04-08
K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.1986-07-29
K844947EMIT ANCILLARY REAGENTSSyva Co.1985-06-28
K844949SYVA SAMPLE SEALSyva Co.1985-02-15
K800556DIFFERENTIAL REFRACTIVE INDEX DETECTORHewlett-Packard Co.1980-03-25
K800516DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.E.I. Dupont DE Nemours & Co., Inc.1980-03-19
K800289LDC SPECTROMONITOR IIILaboratory Data Control1980-02-26
K800046LDC CHROMATOGRAPHY ACCESSORY MODULE BLaboratory Data Control1980-02-25
K800048LDC CONSTAMETRIC III HIGHT PRESS. SOL.Laboratory Data Control1980-01-29
K800047LDC UVIII FIXED WAVELENGTH ULTRAVIOLETLaboratory Data Control1980-01-21
K791661SYSTEM CONTROLLER 720 SERIESWaters Assoc., Inc.1979-09-24