FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ARX Viral Transport Media Collection and Transport System
K Number: K231843
·
Decision Mar 19, 2024
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
2
Review Days
271
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Basic Information
- Device Name
- ARX Viral Transport Media Collection and Transport System
- K Number
- K231843
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2390
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Arx Sciences, Inc.
- Date Received
- June 22, 2023
- Decision Date
- March 19, 2024
- Product Code
- JSM
- 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 |
|---|---|---|---|
| JSM | Culture Media, Non-Propagating Transport | FDA class 1 | Microbiology |
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Other Clearances by Arx Sciences, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K222613 | ARX Liquid Amies Collection & Transport System | Mar 27, 2024 | Substantially Equivalent |