FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EASYTOUCH BUN REAGENT SET

K Number: K832749 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
19
Review Days
60

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EASYTOUCH BUN REAGENT SET
K Number
K832749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Worthington Diagnostic Systems
Date Received
August 15, 1983
Decision Date
October 14, 1983
Product Code
CDQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDQ), ordered by most recent decision date.

View all

Other Clearances by Worthington Diagnostic Systems

K Number Device Name
K833708 COMPUR* M1000 HEMOGLOBIN & ERYTHROCYTE
K832748 COMPUR* EASYTOUCH TOTAL BILIRUBIN
K832427 EASYTOUCH TROMBOPLASTIN REAGENT
K832785 COMPUR* EASY TOUCH URIC ACID REAGENT
K832750 EASYTOUCH HEMOGLOBIN REAGENT
K832426 EASYTOUCH TRIGLYCERIDES REAGENT SET
K831477 DEMAND ANALYZER SYSTEM
K831318 COMPUR* M1100 HEMATRCRIT SYSTEM
K831227 COMPUR EASY TOUCH CHEMISTRY ANALYZER-
K831102 TIA-IGA REAGENT & CALIBRATOR SETS
Search all 19 clearances from Worthington Diagnostic Systems →