FDA 510(k)

Medline Universal Grounding Pad

N.º K: K212093 · 2022-01-14

Fecha de decisión2022-01-14

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Medline Universal Grounding Pad is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2022-01-14 under 510(k) number K212093. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Medline Universal Grounding Pad?

Medline Universal Grounding Pad is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Medline Industries, Inc.. The 510(k) number is K212093.

When did Medline Universal Grounding Pad receive FDA 510(k) clearance?

Medline Universal Grounding Pad received FDA 510(k) clearance on 2022-01-14, under 510(k) number K212093.

Who is the listed applicant for Medline Universal Grounding Pad?

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

What is the FDA product code for Medline Universal Grounding Pad?

The FDA product code for Medline Universal Grounding Pad is GEI.

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Fuente oficial

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