FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Fast PCR Mini Respiratory Panel
K Number: K252932
·
Decision Jun 12, 2026
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
1
Review Days
270
Basic Information
- Device Name
- Fast PCR Mini Respiratory Panel
- K Number
- K252932
- Device Class
- FDA class 2
- Clearance Type
- Dual Track
- Regulation Number
- 866.3981
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Autonomous Medical Devices Incorporated
- Date Received
- September 15, 2025
- Decision Date
- June 12, 2026
- Product Code
- QOF
- 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 |
|---|---|---|---|
| QOF | Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents | FDA class 2 | Microbiology |
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