FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG
K Number: K140354
·
Decision May 9, 2014
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
44
Applicant Total
17
Review Days
86
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Basic Information
- Device Name
- ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG
- K Number
- K140354
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3390
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Abbott Molecular, Inc.
- Date Received
- February 12, 2014
- Decision Date
- May 9, 2014
- Product Code
- LSL
- 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 |
|---|---|---|---|
| LSL | Dna-Reagents, Neisseria | FDA class 2 | Microbiology |
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|---|---|---|---|
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| K241921 | Alinity m BKV | Mar 24, 2025 | Substantially Equivalent |
| K241573 | Alinity m Resp-4-Plex | Feb 14, 2025 | Substantially Equivalent |
| K233349 | Alinity m HSV 1 & 2 / VZV | May 3, 2024 | Substantially Equivalent |
| K222379 | Alinity m STI Assay | Mar 3, 2023 | Substantially Equivalent |
| K212778 | Alinity m EBV AMP Kit (List No. 09N43-095), Alinity m EBV CTRL Kit (List No. 09N43-085), Alinity m EBV CAL Kit (List No. 09N43-075) | Jul 15, 2022 | Substantially Equivalent |
| K202977 | Alinity m STI Assay | Apr 29, 2022 | Substantially Equivalent |
| K131508 | VYSIS D7S486/CEP 7 FISH PROBE KIT | Sep 13, 2013 | Substantially Equivalent |