Philips BlueControl— 510(k) K171055
Substantially EquivalentPhilips Electronics Nederland B.V.
FDA 510(k) clearance K171055 for Philips BlueControl, Substantially Equivalent on 2017-07-06. Applicant: Philips Electronics Nederland B.V.. Device class: 2.
Clearance details
- Applicant
- Philips Electronics Nederland B.V.
- Product code
- Code ONE
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Eindhoven, NL
Recent devices under product code ONE
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