FDA 510(k)

SkinStylus SteriLock MicroSystem (MP1209SL)

K号: K253002 · 2026-02-19

决定日期2026-02-19

产品代码QAI

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决定实质等同

器械摘要

SkinStylus SteriLock MicroSystem (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 2026-02-19 under 510(k) number K253002. 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 (MP1209SL)?

SkinStylus SteriLock MicroSystem (MP1209SL) is a medical device that received FDA 510(k) clearance on 2026-02-19. The listed applicant is Esthetic Medical, Inc.. The 510(k) number is K253002.

When did SkinStylus SteriLock MicroSystem (MP1209SL) receive FDA 510(k) clearance?

SkinStylus SteriLock MicroSystem (MP1209SL) received FDA 510(k) clearance on 2026-02-19, under 510(k) number K253002.

Who is the listed applicant for SkinStylus SteriLock MicroSystem (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 (MP1209SL)?

The FDA product code for SkinStylus SteriLock MicroSystem (MP1209SL) is QAI.

列明Esthetic Medical, Inc.为申报人的其他记录

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K231073SkinStylus SteriLock® MicroSystem，型号：MP1209SL

官方来源

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