FDA 510(k)

REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)

N.º K: K254210 · 2026-09-25

Fecha de decisión2026-09-25

Código de productoNPM

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is the device name listed in this FDA 510(k) record. The listed applicant is Hyundai Bioland Co., Ltd.. It received FDA 510(k) clearance on 2026-09-25 under 510(k) number K254210. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?

REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Hyundai Bioland Co., Ltd.. The 510(k) number is K254210.

When did REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) receive FDA 510(k) clearance?

REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) received FDA 510(k) clearance on 2026-09-25, under 510(k) number K254210.

Who is the listed applicant for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?

The FDA 510(k) record lists Hyundai Bioland Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?

The FDA product code for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is NPM.

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Fuente oficial

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