ELECTRONIC PULSE MASSAGER— 510(k) K131933
Substantially EquivalentGurin Products, LLC
FDA 510(k) clearance K131933 for ELECTRONIC PULSE MASSAGER, Substantially Equivalent on 2013-12-20. Applicant: Gurin Products, LLC. Device class: 2.
Clearance details
- Applicant
- Gurin Products, LLC
- Product code
- 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
- Tustin, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.