ACUBAND ACUPRESSURE WRIST BAND DEVICE— 510(k) K053509
Substantially EquivalentAcuband, Inc.
FDA 510(k) clearance K053509 for ACUBAND ACUPRESSURE WRIST BAND DEVICE, Substantially Equivalent on 2006-08-16. Applicant: Acuband, Inc..
Clearance details
- Applicant
- Acuband, Inc.
- Product code
- Code MVV
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Little Silver, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.