PulseRelief— 510(k) K151035
Substantially EquivalentPhilips Consumer Lifestyle
FDA 510(k) clearance K151035 for PulseRelief, Substantially Equivalent on 2015-07-21. Applicant: Philips Consumer Lifestyle. Device class: 2.
Clearance details
- Applicant
- Philips Consumer Lifestyle
- 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
- Stamford, CT, US
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