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

CELLSEARCH CIRCULATING TUMOR CELL KIT

K Number: K073338 · Decision Feb 26, 2008
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
12
Applicant Total
12
Review Days
90

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
CELLSEARCH CIRCULATING TUMOR CELL KIT
K Number
K073338
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6020
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Veridex, LLC
Date Received
November 28, 2007
Decision Date
February 26, 2008
Product Code
NQI
Advisory Committee
Immunology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
NQI System, Immunomagnetic, Circulating Cancer Cell, Enumeration

Similar 510(k) Clearances

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

View all

Other Clearances by Veridex, LLC

K Number Device Name
K130794 CELLTRACKS ANALYZER II SYSTEM
K122821 CELLTRACKS AUTOPREP SYSTEM
K110406 CELLTRACKS AUTOPREP SYSTEM
K113181 CELLTRACKS ANALYER II
K103502 CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001
K100684 CELLTRACKS AUTOPREP SYSTEM MODEL:9541
K071729 CELLSEARCH CIRCULATING TUMOR CELL KIT
K062013 CELLSEARCH CIRCULATING TUMOR CELL KIT
K052191 MODIFICATION TO CELLSEARCH CIRCULATING TUMOR CELL KIT
K050245 CELLSEARCH CIRCULATING TUMOR CELL KIT
Search all 12 clearances from Veridex, LLC →