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

HDL SINGLES

K Number: K895381 · Decision Nov 8, 1989
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
65
Applicant Total
22
Review Days
71

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Basic Information

Device Name
HDL SINGLES
K Number
K895381
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Trace America, Inc.
Date Received
August 29, 1989
Decision Date
November 8, 1989
Product Code
LBR
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
LBR Ldl & Vldl Precipitation, Hdl

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K974620 AMMONIA-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
K972297 AMYLASE-INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K971477 UREA (UREA NITROGEN) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
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K962723 TRACE HDL CHOLESTEROL - AUTOMATED (HOMOGEN
Search all 22 clearances from Trace America, Inc. →