510(k) K771314

Device
GLUCOSE REAGENT (O-TOLUIDINE)
Applicant
Mallinckrodt Critical Care
510(k) number
K771314
Product code
CGE
Decision
Substantially Equivalent (SESE)
Decision date
1977-08-03
Date received
1977-07-18
Regulation
862.1345
Classification name
Orthotoluidine, Glucose
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Third party reviewed
N

Applicant Contact#

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

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code CGE#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K890335SODIUM HYDROXIDE SOLUTION, CREATININE REAG./DILU.Alpkem Corp.1989-02-17
K855185GLUCOSE REAGENT SETTechnostics Intl.1986-01-22
K850930GLUCOSEDilab, Inc.1985-06-10
K841054DIRECT GLUCOSE REAGENT SETMedical Specialties, Inc.1984-05-01
K821198DIRECT GLUCOSE REAGENT SETOmega Medical Electronics1982-07-13
K811883KING DIAGNOSTICS GLUCOSE-O TESTKing Diagnostics, Inc.1981-07-23
K8100896% ORTHO LOLIUDINE REAGENT IN GLACID ACIAnco Medical Reagents & Assoc.1981-01-26
K790319ORTHO-TOLUIDINE REAGENT SETFisher Scientific Co., LLC1979-03-21
K781308GLUCOLOURAnalytical & Research Chemicals, Inc.1978-08-31
K771091UNIPAK GLUCOSEHarleco1977-07-21
K770455GLUCOSE PROCEDURE, TEKPOINT DIRECTIcn Pharmaceuticals, Inc.1977-05-03