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

ATAC PAK DIRECT HDL REAGENT AND ATAC DIRECT HDL CALIBRATOR KITS

K Number: K013152 · Decision Nov 9, 2001
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
12
Review Days
50

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Basic Information

Device Name
ATAC PAK DIRECT HDL REAGENT AND ATAC DIRECT HDL CALIBRATOR KITS
K Number
K013152
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elan Holdings, Inc.
Date Received
September 20, 2001
Decision Date
November 9, 2001
Product Code
LBS
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
LBS Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LBS), ordered by most recent decision date.

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Other Clearances by Elan Holdings, Inc.

K Number Device Name
K012474 ATAC PAK CPK REAGENT KIT
K010488 ATAC PAK AST REAGENT KIT
K000958 ATAC PAK BUN REAGENT AND ATAC CALIBRATOR KITS
K000900 ATAC PAK CHOLESTEROL REAGENT AND ATAC CALLIBRATOR KITS
K992842 HICHEM ISE ELECTROLYTE REFERENCE
K992844 HICHEM ISE ELECTROLYTE BUFFER
K992846 HICHEM TOTAL PROTEIN REAGENT
K992845 HICHEM CALIBRATOR 1 KIT, HICHEM CALIBRATOR 2 KIT, HICHEM CALIBRATOR 3 KIT, CALIBRATION STANDARDS KIT
K992847 HICHEM BUN REAGENT
K991789 ATAC-PAK DIRECT HDL CHOLESTEROL REAGENT AND ATAC HDL-C CALIBRATOR KITS
Search all 12 clearances from Elan Holdings, Inc. →