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FDA 510(k)

SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K022400 · 2002-08-06

ApplicantToshiba America Medical Systems, In.C
Decision Date2002-08-06
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 2002-08-06 under 510(k) number K022400. 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 SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM?

SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-06. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K022400.

When did SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 2002-08-06, under 510(k) number K022400.

Who is the listed applicant for SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for SSA-700A, APLIO DIAGNOSTIC ULTRASOUND SYSTEM is IYN.

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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.

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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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