FDA 510(k)

GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM

K-Number: K032620 · 2003-10-10

Decision Date2003-10-10

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM 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 2003-10-10 under 510(k) number K032620. 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 BT03 ULTRASOUND SYSTEM?

GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-10. The listed applicant is General Electric Co.. The 510(k) number is K032620.

When did GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM receive FDA 510(k) clearance?

GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM received FDA 510(k) clearance on 2003-10-10, under 510(k) number K032620.

Who is the listed applicant for GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM?

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 BT03 ULTRASOUND SYSTEM?

The FDA product code for GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM 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.