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FDA 510(k)

Slim UP ULTRA

K-Number: K151722 · 2016-03-18

ApplicantAime Medical, Inc.
Decision Date2016-03-18
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Slim UP ULTRA is a medical device manufactured by Aime Medical, Inc.. It received FDA 510(k) clearance on 2016-03-18 under approval number K151722. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Slim UP ULTRA?

Slim UP ULTRA is a medical device that received FDA 510(k) clearance on 2016-03-18. It is manufactured by Aime Medical, Inc.. The 510(k) number is K151722.

When was Slim UP ULTRA approved by the FDA?

Slim UP ULTRA received FDA 510(k) clearance on 2016-03-18, under approval number K151722.

What company makes Slim UP ULTRA?

Slim UP ULTRA is manufactured by Aime Medical, Inc..

What is the FDA product code for Slim UP ULTRA?

The FDA product code for Slim UP ULTRA is NGX.

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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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