FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SOFIA(R) RSV FIA
K Number: K130398
·
Decision Aug 13, 2013
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
31
Applicant Total
93
Review Days
175
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Basic Information
- Device Name
- SOFIA(R) RSV FIA
- K Number
- K130398
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3480
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Quidel Corp.
- Date Received
- February 19, 2013
- Decision Date
- August 13, 2013
- Product Code
- GQG
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| GQG | Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus | FDA class 1 | Microbiology |
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Other Clearances by Quidel Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K131813 | QUIDEL MOLECULAR RSV + HMPV ASSAY | Sep 6, 2013 | Substantially Equivalent |
| K131728 | QUIDEL MOLECULAR INFLUENZA A + B ASSAY | Aug 29, 2013 | Substantially Equivalent |
| K131166 | SOFIA(R) HCG FIA | Aug 2, 2013 | Substantially Equivalent |
| K131606 | SOFIA INFLUENZA A+B FIA | Jul 5, 2013 | Substantially Equivalent |
| K131619 | QUICKVUE INFLUENZA A+B | Jun 28, 2013 | Substantially Equivalent |
| K122189 | QUIDEL MOLECULAR RSV + HMPV ASSAY | Mar 8, 2013 | Substantially Equivalent |
| K123998 | QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY | Mar 8, 2013 | Substantially Equivalent |
| K113777 | QUIDEL MOLECULAR INFLUENZA A+B | Mar 15, 2012 | Substantially Equivalent |
| K112172 | QUIDEL MOLECULAR INFLUENZA A + B ASSAY | Dec 22, 2011 | Substantially Equivalent |
| K112490 | QUIDEL MOLECULAR HMPV ASSAY | Dec 15, 2011 | Substantially Equivalent |