FDA 510(k)

GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04

K-Number: K041688 · 2004-07-08

Decision Date2004-07-08

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04 is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 2004-07-08 under 510(k) number K041688. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04?

GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04 is a medical device that received FDA 510(k) clearance on 2004-07-08. The listed applicant is General Electric Co.. The 510(k) number is K041688.

When did GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04 receive FDA 510(k) clearance?

GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04 received FDA 510(k) clearance on 2004-07-08, under 510(k) number K041688.

Who is the listed applicant for GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04?

The FDA product code for GE VOLUSON 730 PRO/EXPERT UNTRASOUND BT04 is IYN.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.