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

UREA NITROGEN TEST ITEM NUMBER 65408

K Number: K932161 · Decision Sep 8, 1993
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
116
Applicant Total
288
Review Days
127

Basic Information

Device Name
UREA NITROGEN TEST ITEM NUMBER 65408
K Number
K932161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
EM DIAGNOSTIC SYSTEMS, INC.
Date Received
May 4, 1993
Decision Date
September 8, 1993
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

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