LIFENET EXCHANGE SYSTEM
K-Number: K052854 · 2006-01-20
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Device Summary
Frequently Asked Questions
What is the LIFENET EXCHANGE SYSTEM?
LIFENET EXCHANGE SYSTEM is a medical device that received FDA 510(k) clearance on 2006-01-20. The listed applicant is Medtronic Emergency Response Systems, Inc.. The 510(k) number is K052854.
When did LIFENET EXCHANGE SYSTEM receive FDA 510(k) clearance?
LIFENET EXCHANGE SYSTEM received FDA 510(k) clearance on 2006-01-20, under 510(k) number K052854.
Who is the listed applicant for LIFENET EXCHANGE SYSTEM?
The FDA 510(k) record lists Medtronic Emergency Response Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFENET EXCHANGE SYSTEM?
The FDA product code for LIFENET EXCHANGE SYSTEM is MSX.
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 Emergency Response Systems, 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: MSX)
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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