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FDA 510(k)

ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM

K-Number: K032875 · 2003-09-30

ApplicantAloka Co. Ltd USA
Decision Date2003-09-30
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aloka Co. Ltd USA. It received FDA 510(k) clearance on 2003-09-30 under 510(k) number K032875. 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 ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM?

ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2003-09-30. The listed applicant is Aloka Co. Ltd USA. The 510(k) number is K032875.

When did ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM receive FDA 510(k) clearance?

ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM received FDA 510(k) clearance on 2003-09-30, under 510(k) number K032875.

Who is the listed applicant for ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM?

The FDA 510(k) record lists Aloka Co. Ltd USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM?

The FDA product code for ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM is IYO.

Related Clinical Trials

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Other records listing Aloka Co. Ltd USA 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.

K041916ALOKA SSD-ALPHA 5 ULTRASOUND SYSTEM

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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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