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

RDI HOMOGENEOUS HDL CHOLESTEROL TEST

K Number: K973988 · Decision Dec 22, 1997
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
17
Review Days
62

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Basic Information

Device Name
RDI HOMOGENEOUS HDL CHOLESTEROL TEST
K Number
K973988
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Reference Diagnostics, Inc.
Date Received
October 21, 1997
Decision Date
December 22, 1997
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 Reference Diagnostics, Inc.

K Number Device Name
K053211 RDI HSFERRITIN KIT
K053291 FERRITIN CALIBRATOR SET, CATALOG NO. 8203
K052148 TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET
K030044 EXTENDED RANGE HS CRP KIT, CAT NO:9200
K030772 RDI EXTENDED RANGE CRP CALIBRATOR SET
K021609 RDI HS CRP KIT
K021607 RDI HS CRP CALIBRATOR SET
K000783 DIRECT TIBC CALIBRATOR
K000781 DIRECT TIBC KIT
K990216 MAGNETIC TIBC KIT
Search all 17 clearances from Reference Diagnostics, Inc. →