Philips BlueControl— 510(k) K171055

Substantially Equivalent

Philips Electronics Nederland B.V.

FDA 510(k) clearance K171055 for Philips BlueControl, Substantially Equivalent on 2017-07-06. Applicant: Philips Electronics Nederland B.V..

Clearance details

Applicant: Philips Electronics Nederland B.V.
Product code: Code ONE
Advisory panel: General, Plastic Surgery
Date received: 2017-04-10
Decision date: 2017-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eindhoven, NL

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