PATHFINDER
K-Number: K031788 · 2004-09-02
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Device Summary
Frequently Asked Questions
What is the PATHFINDER?
PATHFINDER is a medical device that received FDA 510(k) clearance on 2004-09-02. The listed applicant is Massie Research Laboratories, Inc.. The 510(k) number is K031788.
When did PATHFINDER receive FDA 510(k) clearance?
PATHFINDER received FDA 510(k) clearance on 2004-09-02, under 510(k) number K031788.
Who is the listed applicant for PATHFINDER?
The FDA 510(k) record lists Massie Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATHFINDER?
The FDA product code for PATHFINDER is MXK.
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 Massie Research Laboratories, 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: MXK)
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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