510(k) K780104

Device
ULTRAZYME PLUS HBD
Applicant
HARLECO
510(k) number
K780104
Product code
JMK  
Decision
Substantially Equivalent (SESE)
Decision date
1978-02-13
Date received
1978-01-20
Regulation
862.1380
Classification name
Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase
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 JMK  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K983860MTM BIOSCANNER K TEST STRIPS, CAT # BSA610Polymer Technology Systems, Inc.1999-12-27
K981865MTM BIOSCANNER K TEST STRIPSPolymer Technology Systems, Inc.1999-02-26
K953452KETOREX C SANWAIhara Medics U.S., Inc.1996-05-02
K941427SERUM @-HYDROXYBUTYRATE DEHYDROGENASE (HBDH)Teco Diagnostics1995-03-13
K862319HBDH (OPTIMIZED) REAGENTSigma Chemical Co.1986-07-07
K843774RAICHEM X-HBDH REAGENTReagents Applications, Inc.1984-10-31
K822739AHBDGilford Diagnostics1982-10-18
K821877ULTRAZYME PLUS HBDHarleco Diagnostics1982-07-14
K781720HBDH ENZYME KINETIC REAGENT SETMedical Analysis Systems, Inc.1978-11-03
K780073HBDH REAGENT SETMedical Analysis Systems, Inc.1978-02-13
K780042HYDORRYBUTYRATE DEHYDROGENASEBeckman Instruments, Inc.1978-02-01
K772033GEMSAEC APPLI. FOR ULTRAZYME PLUS ALP*Harleco1977-11-17
K771474MULTISTAT III X-HBDH TESTInstrumentation Laboratory CO1977-09-13
K770871ULTRAZYME PLUS HBDHarleco1977-07-14
K760023ULTRAZYME HBDHarleco1976-08-26

Legacy Summary#

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FDA Review#

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