FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Visby Medical Sexual Health Test
K Number: K220407
·
Decision Mar 7, 2023
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
22
Applicant Total
2
Review Days
386
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Basic Information
- Device Name
- Visby Medical Sexual Health Test
- K Number
- K220407
- Device Class
- FDA class 2
- Clearance Type
- Dual Track
- Regulation Number
- 866.3393
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Visby Medical
- Date Received
- February 14, 2022
- Decision Date
- March 7, 2023
- Product Code
- QEP
- 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 |
|---|---|---|---|
| QEP | Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections | FDA class 2 | Microbiology |
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Other Clearances by Visby Medical
| K Number | Device Name | ||
|---|---|---|---|
| K200748 | Visby Medical Sexual Health | Aug 26, 2021 | Substantially Equivalent |