FDA 510(k)

Allerhope Prueba de Alergia de la Piel

N.º K: K162917 · 2017-08-17

SolicitanteProcare Industrial Co., Limited

Fecha de decisión2017-08-17

Código de productoSCL

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Allerhope Allergy Skin Tester is the device name listed in this FDA 510(k) record. The listed applicant is Procare Industrial Co., Limited. It received FDA 510(k) clearance on 2017-08-17 under 510(k) number K162917. The device is classified under product code SCL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Allerhope Allergy Skin Tester?

Allerhope Allergy Skin Tester is a medical device that received FDA 510(k) clearance on 2017-08-17. The listed applicant is Procare Industrial Co., Limited. The 510(k) number is K162917.

When did Allerhope Allergy Skin Tester receive FDA 510(k) clearance?

Allerhope Allergy Skin Tester received FDA 510(k) clearance on 2017-08-17, under 510(k) number K162917.

Who is the listed applicant for Allerhope Allergy Skin Tester?

The FDA 510(k) record lists Procare Industrial Co., Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Allerhope Allergy Skin Tester?

The FDA product code for Allerhope Allergy Skin Tester is SCL.

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Dispositivos relacionados (Código: SCL)

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Fuente oficial

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