FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RDI HS CRP KIT

K Number: K021609 · Decision Jun 27, 2002
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
17
Review Days
42

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Basic Information

Device Name
RDI HS CRP KIT
K Number
K021609
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Reference Diagnostics, Inc.
Date Received
May 16, 2002
Decision Date
June 27, 2002
Product Code
DCK
Advisory Committee
Immunology
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

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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
K021607 RDI HS CRP CALIBRATOR SET
K000783 DIRECT TIBC CALIBRATOR
K000781 DIRECT TIBC KIT
K990216 MAGNETIC TIBC KIT
K984107 RDI DIRECT LDL CHOLESTEROL TEST
Search all 17 clearances from Reference Diagnostics, Inc. →