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FDA 510(k)

CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM

K-Number: K061488 · 2006-06-30

Decision Date2006-06-30
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Shantou Institute of Ultrasonic Instruments (Siui. It received FDA 510(k) clearance on 2006-06-30 under 510(k) number K061488. 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 CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM?

CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-06-30. The listed applicant is Shantou Institute of Ultrasonic Instruments (Siui. The 510(k) number is K061488.

When did CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM receive FDA 510(k) clearance?

CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM received FDA 510(k) clearance on 2006-06-30, under 510(k) number K061488.

Who is the listed applicant for CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM?

The FDA 510(k) record lists Shantou Institute of Ultrasonic Instruments (Siui as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM?

The FDA product code for CTS-5500/CTS-6600 ULTRASONIC PULSED ECHO IMAGING SYSTEM is IYN.

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 Shantou Institute of Ultrasonic Instruments (Siui 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.

Related Devices (Code: IYN)

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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