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FDA 510(k)

2K-QDA MOTION/GAIT ANALYSIS SYSTEM

K-Number: K880631 · 1988-04-21

Decision Date1988-04-21
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

2K-QDA MOTION/GAIT ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Human Performance Technologies, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K880631. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2K-QDA MOTION/GAIT ANALYSIS SYSTEM?

2K-QDA MOTION/GAIT ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Human Performance Technologies, Inc.. The 510(k) number is K880631.

When did 2K-QDA MOTION/GAIT ANALYSIS SYSTEM receive FDA 510(k) clearance?

2K-QDA MOTION/GAIT ANALYSIS SYSTEM received FDA 510(k) clearance on 1988-04-21, under 510(k) number K880631.

Who is the listed applicant for 2K-QDA MOTION/GAIT ANALYSIS SYSTEM?

The FDA 510(k) record lists Human Performance Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 2K-QDA MOTION/GAIT ANALYSIS SYSTEM?

The FDA product code for 2K-QDA MOTION/GAIT ANALYSIS SYSTEM 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 Human Performance Technologies, 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: 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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