FDA 510(k)

Proton Positioing and Immobilization Devices

Numéro K : K180021 · 2018-06-29

DemandeurMedtec Inc Dba Civco Medical Solutions and Civco Radiotherap

Date de décision2018-06-29

Code produitIYE

Comité consultatifRA

DécisionSubstantially Equivalent

Résumé du dispositif

Proton Positioing and Immobilization Devices is the device name listed in this FDA 510(k) record. The listed applicant is Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap. It received FDA 510(k) clearance on 2018-06-29 under 510(k) number K180021. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Proton Positioing and Immobilization Devices?

Proton Positioing and Immobilization Devices is a medical device that received FDA 510(k) clearance on 2018-06-29. The listed applicant is Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap. The 510(k) number is K180021.

When did Proton Positioing and Immobilization Devices receive FDA 510(k) clearance?

Proton Positioing and Immobilization Devices received FDA 510(k) clearance on 2018-06-29, under 510(k) number K180021.

Who is the listed applicant for Proton Positioing and Immobilization Devices?

The FDA 510(k) record lists Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Proton Positioing and Immobilization Devices?

The FDA product code for Proton Positioing and Immobilization Devices is IYE.

Essais cliniques associés

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Source officielle

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