VERABAND™
FDA 510(k) clearance K233987 · decided 2024-06-17
Clearance details
- K-number
- K233987
- Device name
- VERABAND™
- Applicant
- Arbor Medical Innovations, LLC
- Decision
- Substantially Equivalent
- Date received
- 2023-12-18
- Decision date
- 2024-06-17
- Days to decision
- 182 days
- Clearance type
- Traditional
- Product code
- LEL
- Device class
- 2
- Regulation number
- 882.5050
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Saline, MI, US
- Third-party review
- No
- Expedited review
- No
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| CADWELL LIMB MOVEMENT MODULE (K040986) | Cadwell Laboratories, Inc. | 2004-07-01 |
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Recalls involving this device
No recalls on record reference this clearance.