PACIFIC PLUS
K-Number: K123358 · 2013-01-29
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Device Summary
Frequently Asked Questions
What is the PACIFIC PLUS?
PACIFIC PLUS is a medical device that received FDA 510(k) clearance on 2013-01-29. The listed applicant is Medtronic Vascular. The 510(k) number is K123358.
When did PACIFIC PLUS receive FDA 510(k) clearance?
PACIFIC PLUS received FDA 510(k) clearance on 2013-01-29, under 510(k) number K123358.
Who is the listed applicant for PACIFIC PLUS?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PACIFIC PLUS?
The FDA product code for PACIFIC PLUS is LIT.
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 Vascular 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: LIT)
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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