FDA 510(k)

Deka Tiac 1

N.º K: K183371 · 2019-12-03

SolicitanteEl..En. Electroic Engineering Spa

Fecha de decisión2019-12-03

Código de productoPBX

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Deka Tiac 1 is the device name listed in this FDA 510(k) record. The listed applicant is El..En. Electroic Engineering Spa. It received FDA 510(k) clearance on 2019-12-03 under 510(k) number K183371. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Deka Tiac 1?

Deka Tiac 1 is a medical device that received FDA 510(k) clearance on 2019-12-03. The listed applicant is El..En. Electroic Engineering Spa. The 510(k) number is K183371.

When did Deka Tiac 1 receive FDA 510(k) clearance?

Deka Tiac 1 received FDA 510(k) clearance on 2019-12-03, under 510(k) number K183371.

Who is the listed applicant for Deka Tiac 1?

The FDA 510(k) record lists El..En. Electroic Engineering Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Deka Tiac 1?

The FDA product code for Deka Tiac 1 is PBX.

Dispositivos relacionados (Código: PBX)

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Fuente oficial

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