XPS 3000 SYSTEM
K-Number: K041413 · 2004-07-12
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Device Summary
Frequently Asked Questions
What is the XPS 3000 SYSTEM?
XPS 3000 SYSTEM is a medical device that received FDA 510(k) clearance on 2004-07-12. The listed applicant is Medtronic Xomed, Inc.. The 510(k) number is K041413.
When did XPS 3000 SYSTEM receive FDA 510(k) clearance?
XPS 3000 SYSTEM received FDA 510(k) clearance on 2004-07-12, under 510(k) number K041413.
Who is the listed applicant for XPS 3000 SYSTEM?
The FDA 510(k) record lists Medtronic Xomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XPS 3000 SYSTEM?
The FDA product code for XPS 3000 SYSTEM is ERL.
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 Medtronic Xomed, 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: ERL)
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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