FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ID NOW Influenza A & B 2
K Number: K190204
·
Decision Mar 18, 2019
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
19
Applicant Total
17
Review Days
42
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Basic Information
- Device Name
- ID NOW Influenza A & B 2
- K Number
- K190204
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 866.3980
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Alere Scarborough, Inc.
- Date Received
- February 4, 2019
- Decision Date
- March 18, 2019
- Product Code
- OZE
- 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 |
|---|---|---|---|
| OZE | Influenza A And Influenza B Multiplex Nucleic Acid Assay | FDA class 2 | Microbiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (OZE), ordered by most recent decision date.
CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)
FDA 510(k)
FDA Class 2
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CDC Human Influenza Virus Real-time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A Subtyping Kit (VER 4); Influenza B Lineage Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)
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CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit (Ver4)
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Lyra Influenza A+B Assay
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FDA Class 2
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ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2
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·Microbiology
CDC Human Influenza Virus Real-time RT-PCR Diagnostic Panel, Influenza A/B Typing Kit, CDC Human Influenza Virus Real-time RT-PCR Diagnostic Panel, Influenza A Subtyping Kit, CDC Human Influenza Virus Real-time RT-PCR, Influenza A/H5 Subtyping Kit
FDA 510(k)
FDA Class 2
·Microbiology
Other Clearances by Alere Scarborough, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| DEN180014 | WOUNDCHEK Bacterial Status | Dec 2, 2019 | Unknown |
| K181853 | Alere BinaxNOW Influenza A & B Card 2, Alere Reader | Aug 8, 2018 | Substantially Equivalent |
| K173653 | Alere i Strep A 2, Alere i instrument, Alere i Strep A 2 Control Swab Kit | May 2, 2018 | Substantially Equivalent |
| K173932 | Alere i Influenza A & B, Alere i Strep A, Alere i RSV, Alere i Influenza A & B 2 | Jan 26, 2018 | Substantially Equivalent |
| K173502 | Alere BinaxNOW Influenza A & B Card 2, Alere Reader, Alere BinaxNOW Influenza A & B Card 2 Control Swab Kit | Dec 13, 2017 | Substantially Equivalent |
| K171792 | Alere i Influenza A & B 2, Alere i Instrument, Alere i Influenza A & B Control Swab Kit | Sep 29, 2017 | Substantially Equivalent |
| K162642 | Alere BinaxNOW Influenza A & B Card 2, Alere Reader, Alere BinaxNOW Influenza A & B Card 2 Control Swab Kit | Apr 10, 2017 | Substantially Equivalent |
| K163266 | Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument | Dec 21, 2016 | Substantially Equivalent |
| K161375 | Alere i RSV, Alere i Instrument, Alere i RSV Control Swab Kit | Aug 18, 2016 | Substantially Equivalent |
| K161364 | BinaxNOW G6PD Test | Jun 17, 2016 | Substantially Equivalent |