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FDA 510(k)

MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION

K-Number: K063184 · 2006-11-03

ApplicantToshiba America Medical Systems, In.C
Decision Date2006-11-03
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION 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 2006-11-03 under 510(k) number K063184. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION?

MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 2006-11-03. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K063184.

When did MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION receive FDA 510(k) clearance?

MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION received FDA 510(k) clearance on 2006-11-03, under 510(k) number K063184.

Who is the listed applicant for MODEL CVV-001A VESSEL 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 MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION?

The FDA product code for MODEL CVV-001A VESSEL VIEW SOFTWARE OPTION is JAK.

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Related Devices (Code: JAK)

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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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