FDA 510(k)

Fujifilm Sonosite Vevo MD Imaging System

K-Nummer: K160674 · 2016-04-19

Entscheidungsdatum2016-04-19

ProduktcodeIYN

BeratungsausschussRA

EntscheidungSubstantially Equivalent

Produktübersicht

Fujifilm Sonosite Vevo MD Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is FUJIFILM Sonosite, Inc.. It received FDA 510(k) clearance on 2016-04-19 under 510(k) number K160674. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Fujifilm Sonosite Vevo MD Imaging System?

Fujifilm Sonosite Vevo MD Imaging System is a medical device that received FDA 510(k) clearance on 2016-04-19. The listed applicant is FUJIFILM Sonosite, Inc.. The 510(k) number is K160674.

When did Fujifilm Sonosite Vevo MD Imaging System receive FDA 510(k) clearance?

Fujifilm Sonosite Vevo MD Imaging System received FDA 510(k) clearance on 2016-04-19, under 510(k) number K160674.

Who is the listed applicant for Fujifilm Sonosite Vevo MD Imaging System?

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

What is the FDA product code for Fujifilm Sonosite Vevo MD Imaging System?

The FDA product code for Fujifilm Sonosite Vevo MD Imaging System is IYN.

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Weitere Einträge mit FUJIFILM Sonosite, Inc. als Antragsteller

K260595Sonosite iLOOK Ultrasound System K253448Sonosite MT Ultrasound System K251106Sonosite LX and Sonosite PX Ultrasound Systems K251830Sonosite LX Ultrasound System K233597Sonosite LX Ultrasound System K213763Sonosite PX Ultrasound System

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Verwandte Geräte (Code: IYN)

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