Class Class II

Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) (K243030)

K243030 2024-10-25 Special
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Description

Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) by Ulike Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243030
Clearance Date2024-10-25
Clearance TypeSpecial
Product CodeOHT
Regulation Number878.4810

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Predicate lineage for K243030

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) (K243030) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K221553Diamond Air+ (UI04A, UI04B, UI04C)Ulike Co., Ltd.2022

Trace the full predicate network for K243030

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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