FDA 510(k)

SkinStylus SteriLock® MicroSystem，型号：MP1209SL

K号: K231073 · 2023-07-28

决定日期2023-07-28

产品代码QAI

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决定实质等同

器械摘要

SkinStylus SteriLock® MicroSystem, Model Number MP1209SL is the device name listed in this FDA 510(k) record. The listed applicant is Esthetic Medical, Inc.. It received FDA 510(k) clearance on 2023-07-28 under 510(k) number K231073. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SkinStylus SteriLock® MicroSystem, Model Number MP1209SL?

SkinStylus SteriLock® MicroSystem, Model Number MP1209SL is a medical device that received FDA 510(k) clearance on 2023-07-28. The listed applicant is Esthetic Medical, Inc.. The 510(k) number is K231073.

When did SkinStylus SteriLock® MicroSystem, Model Number MP1209SL receive FDA 510(k) clearance?

SkinStylus SteriLock® MicroSystem, Model Number MP1209SL received FDA 510(k) clearance on 2023-07-28, under 510(k) number K231073.

Who is the listed applicant for SkinStylus SteriLock® MicroSystem, Model Number MP1209SL?

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

What is the FDA product code for SkinStylus SteriLock® MicroSystem, Model Number MP1209SL?

The FDA product code for SkinStylus SteriLock® MicroSystem, Model Number MP1209SL is QAI.

列明Esthetic Medical, Inc.为申报人的其他记录

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K253002SkinStylus SteriLock MicroSystem (MP1209SL)

官方来源

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