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

LIPIDIRECT LOW DENSITY LIPOPROTEIN CHOLESTEROL TES

K Number: K893740 · Decision Mar 19, 1990
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
30
Applicant Total
17
Review Days
306

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Basic Information

Device Name
LIPIDIRECT LOW DENSITY LIPOPROTEIN CHOLESTEROL TES
K Number
K893740
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Reference Diagnostics, Inc.
Date Received
May 17, 1989
Decision Date
March 19, 1990
Product Code
MRR
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
MRR System, Test, Low Density, Lipoprotein

Similar 510(k) Clearances

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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. →