VITREA ENDOVASCULAR STENT PLANNING SOFTWARE
K-Number: K091498 · 2009-06-05
Advertisement
Device Summary
Frequently Asked Questions
What is the VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?
VITREA ENDOVASCULAR STENT PLANNING SOFTWARE is a medical device that received FDA 510(k) clearance on 2009-06-05. The listed applicant is Vital Images, Inc.. The 510(k) number is K091498.
When did VITREA ENDOVASCULAR STENT PLANNING SOFTWARE receive FDA 510(k) clearance?
VITREA ENDOVASCULAR STENT PLANNING SOFTWARE received FDA 510(k) clearance on 2009-06-05, under 510(k) number K091498.
Who is the listed applicant for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?
The FDA 510(k) record lists Vital Images, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE?
The FDA product code for VITREA ENDOVASCULAR STENT PLANNING SOFTWARE is LLZ.
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 Vital Images, Inc. 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: LLZ)
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.
Advertisement