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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 the device name listed in this FDA 510(k) record. The listed applicant is Aime Medical, Inc.. It received FDA 510(k) clearance on 2016-03-18 under 510(k) 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. The listed applicant is Aime Medical, Inc.. The 510(k) number is K151722.

When did Slim UP ULTRA receive FDA 510(k) clearance?

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

Who is the listed applicant for Slim UP ULTRA?

The FDA 510(k) record lists Aime Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Slim UP ULTRA?

The FDA product code for Slim UP ULTRA is NGX.

Related Devices (Code: 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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