FDA 510(k)

ViewFinder Software Version 1.1

N.º K: K223501 · 2023-04-21

Fecha de decisión2023-04-21

Código de productoQIH

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

ViewFinder Software Version 1.1 is the device name listed in this FDA 510(k) record. The listed applicant is Elaitra, Ltd.. It received FDA 510(k) clearance on 2023-04-21 under 510(k) number K223501. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ViewFinder Software Version 1.1?

ViewFinder Software Version 1.1 is a medical device that received FDA 510(k) clearance on 2023-04-21. The listed applicant is Elaitra, Ltd.. The 510(k) number is K223501.

When did ViewFinder Software Version 1.1 receive FDA 510(k) clearance?

ViewFinder Software Version 1.1 received FDA 510(k) clearance on 2023-04-21, under 510(k) number K223501.

Who is the listed applicant for ViewFinder Software Version 1.1?

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

What is the FDA product code for ViewFinder Software Version 1.1?

The FDA product code for ViewFinder Software Version 1.1 is QIH.

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Fuente oficial

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