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FDA 510(k)

UST-974-5 CONVEX TRANSDUCER

K-Number: K910153 · 1991-03-29

ApplicantGe Medical Systems Information Technologies
Decision Date1991-03-29
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UST-974-5 CONVEX TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K910153. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UST-974-5 CONVEX TRANSDUCER?

UST-974-5 CONVEX TRANSDUCER is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K910153.

When did UST-974-5 CONVEX TRANSDUCER receive FDA 510(k) clearance?

UST-974-5 CONVEX TRANSDUCER received FDA 510(k) clearance on 1991-03-29, under 510(k) number K910153.

Who is the listed applicant for UST-974-5 CONVEX TRANSDUCER?

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

What is the FDA product code for UST-974-5 CONVEX TRANSDUCER?

The FDA product code for UST-974-5 CONVEX TRANSDUCER is KNG.

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Other records listing Ge Medical Systems Information Technologies as applicant

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Related Devices (Code: KNG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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