CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION
K-Number: K063241 · 2006-11-09
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Device Summary
Frequently Asked Questions
What is the CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION?
CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 2006-11-09. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K063241.
When did CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION receive FDA 510(k) clearance?
CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION received FDA 510(k) clearance on 2006-11-09, under 510(k) number K063241.
Who is the listed applicant for CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION?
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 CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION?
The FDA product code for CSTC-002A, EXTENDED FIELD OF VIEW SOFTWARE OPTION is JAK.
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 Toshiba America Medical Systems, In.C 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: JAK)
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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