FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

URITEK-720+ URINE ANALYZER

K Number: K051526 · Decision Aug 16, 2005
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
45
Applicant Total
50
Review Days
69

Basic Information

Device Name
URITEK-720+ URINE ANALYZER
K Number
K051526
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2900
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
TECO DIAGNOSTICS
Date Received
June 8, 2005
Decision Date
August 16, 2005
Product Code
KQO
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
KQO Automated Urinalysis System

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