FDA 510(k)

ENT Nasopharyngoscope and Accessories

N.º K: K214050 · 2022-07-01

SolicitanteMedimaging Integrated Solution, Inc (Miis)

Fecha de decisión2022-07-01

Código de productoEOB

Comité asesorEN

DecisiónSubstantially Equivalent

Resumen del dispositivo

ENT Nasopharyngoscope and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Medimaging Integrated Solution, Inc (Miis). It received FDA 510(k) clearance on 2022-07-01 under 510(k) number K214050. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ENT Nasopharyngoscope and Accessories?

ENT Nasopharyngoscope and Accessories is a medical device that received FDA 510(k) clearance on 2022-07-01. The listed applicant is Medimaging Integrated Solution, Inc (Miis). The 510(k) number is K214050.

When did ENT Nasopharyngoscope and Accessories receive FDA 510(k) clearance?

ENT Nasopharyngoscope and Accessories received FDA 510(k) clearance on 2022-07-01, under 510(k) number K214050.

Who is the listed applicant for ENT Nasopharyngoscope and Accessories?

The FDA 510(k) record lists Medimaging Integrated Solution, Inc (Miis) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENT Nasopharyngoscope and Accessories?

The FDA product code for ENT Nasopharyngoscope and Accessories is EOB.

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Fuente oficial

Ver en la base de datos de la FDA →

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