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

DART UREA NITROGEN

K Number: K894836 · Decision Oct 30, 1989
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
101
Review Days
91

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
DART UREA NITROGEN
K Number
K894836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Coulter Electronics, Inc.
Date Received
July 31, 1989
Decision Date
October 30, 1989
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 Coulter Electronics, Inc.

K Number Device Name
K923951 CD8 CYTOSPHERES KIT
K930119 COULTER RETIC-C CELL CONTROL
K921279 CD4 CYTOSPHERES KIT
K923530 COULTER MULTI-Q-PREP
K922181 COULTER MH009
K922704 COULTER MAXM W/ AUTOLOADER
K921567 COULTER MH017
K912133 PX COULTER(R) CELL CONTROL
K911385 COULTER(R) MH010
K905771 COULTER DART AST (GOT) REAGENT
Search all 101 clearances from Coulter Electronics, Inc. →