SSA-770A, APLIO VERSION 5.5
K-Number: K041499 · 2004-06-10
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Device Summary
Frequently Asked Questions
What is the SSA-770A, APLIO VERSION 5.5?
SSA-770A, APLIO VERSION 5.5 is a medical device that received FDA 510(k) clearance on 2004-06-10. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K041499.
When did SSA-770A, APLIO VERSION 5.5 receive FDA 510(k) clearance?
SSA-770A, APLIO VERSION 5.5 received FDA 510(k) clearance on 2004-06-10, under 510(k) number K041499.
Who is the listed applicant for SSA-770A, APLIO VERSION 5.5?
The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SSA-770A, APLIO VERSION 5.5?
The FDA product code for SSA-770A, APLIO VERSION 5.5 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 Toshibamedical Systems Corporation 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
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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