Nu-beca Transcutaneous Electrical Nerve Stimulation— 510(k) K223151
Substantially EquivalentNu-Beca & Maxcellent Co.
FDA 510(k) clearance K223151 for Nu-beca Transcutaneous Electrical Nerve Stimulation, Substantially Equivalent on 2023-07-19. Applicant: Nu-Beca & Maxcellent Co.. Device class: 2.
Clearance details
- Applicant
- Nu-Beca & Maxcellent Co.
- Product code
- Product code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taipei, TW
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Data sourced from openFDA. This site is unofficial and independent of the FDA.