VERABAND— 510(k) K233987
Substantially EquivalentArbor Medical Innovations, LLC
FDA 510(k) clearance K233987 for VERABAND, Substantially Equivalent on 2024-06-17. Applicant: Arbor Medical Innovations, LLC. Device class: 2.
Clearance details
- Applicant
- Arbor Medical Innovations, LLC
- Product code
- Code LEL
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Saline, MI, US
Recent devices under product code LEL
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