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

UREA NITROGEN(BUN)

K Number: K863925 · Decision Nov 24, 1986
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
36
Review Days
47

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Basic Information

Device Name
UREA NITROGEN(BUN)
K Number
K863925
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tech-Co, Inc.
Date Received
October 8, 1986
Decision Date
November 24, 1986
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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Other Clearances by Tech-Co, Inc.

K Number Device Name
K921968 IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST
K923376 VISUAL HCG PREGNANCY TEST
K920766 T4 EIA BEAD ASSAY
K920716 DIRECT PREGNANCY TEST
K902574 POTASSIUM REAGENT SET
K901561 IRON/TOTAL IRON BINDING CAPACITY
K883387 ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
K883683 HEMOGLOBIN
K883386 CHLORIDE
K881172 BILIRUBIN (DIRECT)
Search all 36 clearances from Tech-Co, Inc. →