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

QUICKSTART UREA NITROGEN

K Number: K914903 · Decision Dec 31, 1991
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
15
Applicant Total
288
Review Days
60

Basic Information

Device Name
QUICKSTART UREA NITROGEN
K Number
K914903
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
November 1, 1991
Decision Date
December 31, 1991
Product Code
CDN
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
CDN Urease, Photometric, Urea Nitrogen

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K935179 EMDS ALBUMIN (ALB) TEST
K935174 TOTAL PROTEIN TEST (TPRO)
K935136 CHOLESTEROL (CHOL) TEST ITEM NO. 65410
K935175 LACTATE DEHYDROGENASE (LD)
K935177 GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST
K935176 IRON TEST
K935183 EMDS MAGNESIUM (MG) TEST
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