FDA 510(k) FDA class 1 Substantially Equivalent 🇦🇺 Australia

HDL CHOLESTEROL KIT

K Number: K881244 · Decision Jun 10, 1988
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
65
Applicant Total
55
Review Days
79

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Basic Information

Device Name
HDL CHOLESTEROL KIT
K Number
K881244
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Trace Scientific , Ltd.
Date Received
March 23, 1988
Decision Date
June 10, 1988
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

Similar 510(k) Clearances

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Other Clearances by Trace Scientific , Ltd.

K Number Device Name
K982121 ENZYMATIC MITOCHONDRIAL ANTIBODY (M2) REAGENT
K981123 UREA
K962890 CHOLESTEROL-INCORPORATING DYNAMIC STAB TECH (DST)
K961114 AST INCORPORATING DST
K961123 ALT INCORPORATING DST
K952488 TRACE COBAS MIRA RANGE
K932713 TRACE TRANSFERRIN REAGENT
K923322 TRACE ALBUMIN-MR REAGENT
K914731 TRACE GAMMA GT-SS REAGENT
K911866 TRACE TOTAL/DIRECT BILIRUBIN REAGENT
Search all 55 clearances from Trace Scientific , Ltd. →