ElectroTek
K-Number: K170441 · 2017-06-05
ApplicantMobilemedtek
Decision Date2017-06-05
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
ElectroTek is a medical device manufactured by Mobilemedtek. It received FDA 510(k) clearance on 2017-06-05 under approval number K170441. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ElectroTek?
ElectroTek is a medical device that received FDA 510(k) clearance on 2017-06-05. It is manufactured by Mobilemedtek. The 510(k) number is K170441.
When was ElectroTek approved by the FDA?
ElectroTek received FDA 510(k) clearance on 2017-06-05, under approval number K170441.
What company makes ElectroTek?
ElectroTek is manufactured by Mobilemedtek.
What is the FDA product code for ElectroTek?
The FDA product code for ElectroTek is GWQ.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.