FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RDI HSFERRITIN KIT
K Number: K053211
·
Decision Mar 13, 2006
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
17
Review Days
117
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Basic Information
- Device Name
- RDI HSFERRITIN KIT
- K Number
- K053211
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5340
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Reference Diagnostics, Inc.
- Date Received
- November 16, 2005
- Decision Date
- March 13, 2006
- Product Code
- DBF
- Advisory Committee
- Immunology
- Review Advisory Committee
- IM
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DBF | Ferritin, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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Other Clearances by Reference Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K053291 | FERRITIN CALIBRATOR SET, CATALOG NO. 8203 | Mar 13, 2006 | Substantially Equivalent |
| K052148 | TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET | Nov 9, 2005 | Substantially Equivalent |
| K030044 | EXTENDED RANGE HS CRP KIT, CAT NO:9200 | Sep 30, 2003 | Substantially Equivalent |
| K030772 | RDI EXTENDED RANGE CRP CALIBRATOR SET | Apr 11, 2003 | Substantially Equivalent |
| K021609 | RDI HS CRP KIT | Jun 27, 2002 | Substantially Equivalent |
| K021607 | RDI HS CRP CALIBRATOR SET | Jun 27, 2002 | Substantially Equivalent |
| K000783 | DIRECT TIBC CALIBRATOR | May 4, 2000 | Substantially Equivalent |
| K000781 | DIRECT TIBC KIT | May 2, 2000 | Substantially Equivalent |
| K990216 | MAGNETIC TIBC KIT | Feb 16, 1999 | Substantially Equivalent |
| K984107 | RDI DIRECT LDL CHOLESTEROL TEST | Jan 28, 1999 | Substantially Equivalent |