FDA 510(k)

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert

K-Nummer: K213642 · 2022-01-13

Entscheidungsdatum2022-01-13

ProduktcodeIYN

BeratungsausschussRA

EntscheidungSubstantially Equivalent

Produktübersicht

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2022-01-13 under 510(k) number K213642. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert?

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert is a medical device that received FDA 510(k) clearance on 2022-01-13. The listed applicant is GE Healthcare. The 510(k) number is K213642.

When did Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert receive FDA 510(k) clearance?

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert received FDA 510(k) clearance on 2022-01-13, under 510(k) number K213642.

Who is the listed applicant for Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert?

The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert?

The FDA product code for Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert is IYN.

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