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

ATAC DIRECT HDL CHOLESTEROL REAGENT AND ATAC HDL-C CALIBRATOR KITS

K Number: K992029 · Decision Aug 12, 1999
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
65
Applicant Total
13
Review Days
57

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Basic Information

Device Name
ATAC DIRECT HDL CHOLESTEROL REAGENT AND ATAC HDL-C CALIBRATOR KITS
K Number
K992029
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 Diagnostics
Date Received
June 16, 1999
Decision Date
August 12, 1999
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

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

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Other Clearances by Elan Diagnostics

K Number Device Name
K030003 ATAC DIRECT BILIRUBIN REAGENT AND CALIBRATOR
K030014 ATAC TOTAL BILIRUBIN REAGENT
K030621 ATAC CALIBRATOR
K023105 ATAC CALCIUM REAGENT AND ATAC CALIBRATOR
K030010 ATAC PAK MAGNESIUM REAGENT
K030006 ATAC PAK ALBUMIN REAGENT
K030015 ATAC PAK PHOSPHORUS REAGENT
K023407 ATAC PAK CREATININE REAGENT AND ATAC CALIBRATOR
K021385 ATAC PAK BUN REAGENT
K020575 ATAC DIRECT LDL REAGENT AND ATAC DIRECT LDL CALIBRATOR KITS
Search all 13 clearances from Elan Diagnostics →