510(k) K831154

Device
Stratus Phenytoin Fluorometric Enzyme
Applicant
AMERICAN DADE
510(k) number
K831154
Product code
LES
Decision
Substantially Equivalent (SESE)
Decision date
1983-05-16
Date received
1983-04-08
Regulation
862.3350
Classification name
Fluorescent Immunoassay, Diphenylhydantoin
Medical specialty
Clinical Toxicology
Review panel
Clinical Toxicology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LES#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K865102IMMPULSE COATED TUBE PHENYTOIN ASSAY REAGENTSSclavo, Inc.1987-01-13
K844990SYVA ADVANCE EMIT PHENYTOIN ASSAYSyva Co.1985-01-23
K820187SYVA ADVANCE SYS. EMIT,(R)-AED(R) PHENYSyva Co.1982-02-12
K813538PHENYTOIN FLUORESCENT IMMUNOASSAYAmerican Diagnostic Corp.1981-12-31
K811025AMES TDA TM PHENYTOIN TESTMiles Laboratories, Inc.1981-04-29
K801736AMES TDA TM PHENYTOIN TESTMiles Laboratories, Inc.1980-08-20