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FDA 510(k)

SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K973802 · 1998-03-04

Decision Date1998-03-04
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1998-03-04 under 510(k) number K973802. 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 SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM?

SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1998-03-04. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K973802.

When did SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 1998-03-04, under 510(k) number K973802.

Who is the listed applicant for SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM?

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

What is the FDA product code for SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for SHIMASONIC LINEAR/CONVEX DIAGNOSTIC ULTRASOUND SYSTEM is IYO.

Related Clinical Trials

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.

Other records listing Shimadzu Medical Systems as applicant

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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Related Devices (Code: IYO)

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.

Official Source

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

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