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FDA 510(k)

GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K992208 · 1999-07-12

ApplicantGe Medical Systems, Inc.
Decision Date1999-07-12
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, Inc.. It received FDA 510(k) clearance on 1999-07-12 under 510(k) number K992208. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM?

GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1999-07-12. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K992208.

When did GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 1999-07-12, under 510(k) number K992208.

Who is the listed applicant for GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM?

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

What is the FDA product code for GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM is IYO.

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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.

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