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FDA 510(k)

Ultra OTC Facial Toning System

K-Number: K183189 · 2019-04-17

ApplicantMicro Current Technology, Inc.
Decision Date2019-04-17
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Ultra OTC Facial Toning System is a medical device manufactured by Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2019-04-17 under approval number K183189. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultra OTC Facial Toning System?

Ultra OTC Facial Toning System is a medical device that received FDA 510(k) clearance on 2019-04-17. It is manufactured by Micro Current Technology, Inc.. The 510(k) number is K183189.

When was Ultra OTC Facial Toning System approved by the FDA?

Ultra OTC Facial Toning System received FDA 510(k) clearance on 2019-04-17, under approval number K183189.

What company makes Ultra OTC Facial Toning System?

Ultra OTC Facial Toning System is manufactured by Micro Current Technology, Inc..

What is the FDA product code for Ultra OTC Facial Toning System?

The FDA product code for Ultra OTC Facial Toning System is NFO.

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Other Devices by Micro Current Technology, Inc.

K181062Ultra Facial Toning System K233525MF SC Facial Toning System K233095S21 OTC Transcutaneous Electrical Nerve Stimulator K252218MF SC GEN2 Facial Toning System

Related Devices (Code: NFO)

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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.

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