FOOTTRAK
K-Number: K890075 · 1989-02-03
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Device Summary
Frequently Asked Questions
What is the FOOTTRAK?
FOOTTRAK is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Motion Analysis Corp.. The 510(k) number is K890075.
When did FOOTTRAK receive FDA 510(k) clearance?
FOOTTRAK received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890075.
Who is the listed applicant for FOOTTRAK?
The FDA 510(k) record lists Motion Analysis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOOTTRAK?
The FDA product code for FOOTTRAK is LXJ.
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 Motion Analysis Corp. 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: LXJ)
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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