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FDA 510(k)

sensiLift

K-Number: K170499 · 2017-06-15

Decision Date2017-06-15
Product CodePAY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

sensiLift is a medical device manufactured by El Global Trade, Ltd.. It received FDA 510(k) clearance on 2017-06-15 under approval number K170499. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the sensiLift?

sensiLift is a medical device that received FDA 510(k) clearance on 2017-06-15. It is manufactured by El Global Trade, Ltd.. The 510(k) number is K170499.

When was sensiLift approved by the FDA?

sensiLift received FDA 510(k) clearance on 2017-06-15, under approval number K170499.

What company makes sensiLift?

sensiLift is manufactured by El Global Trade, Ltd..

What is the FDA product code for sensiLift?

The FDA product code for sensiLift is PAY.

Other Devices by El Global Trade, Ltd.

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Related Devices (Code: PAY)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.