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FDA 510(k)

PEAK MOTUS

K-Number: K030714 · 2003-05-16

ApplicantPeak Performance Technologies, Inc.
Decision Date2003-05-16
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PEAK MOTUS is the device name listed in this FDA 510(k) record. The listed applicant is Peak Performance Technologies, Inc.. It received FDA 510(k) clearance on 2003-05-16 under 510(k) number K030714. 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 PEAK MOTUS?

PEAK MOTUS is a medical device that received FDA 510(k) clearance on 2003-05-16. The listed applicant is Peak Performance Technologies, Inc.. The 510(k) number is K030714.

When did PEAK MOTUS receive FDA 510(k) clearance?

PEAK MOTUS received FDA 510(k) clearance on 2003-05-16, under 510(k) number K030714.

Who is the listed applicant for PEAK MOTUS?

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

What is the FDA product code for PEAK MOTUS?

The FDA product code for PEAK MOTUS is LXJ.

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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.

K192474VERAReflexion Health, Inc.K182333VeraReflexion Health, Inc.K180880DARI HealthScientific Analytics, Inc.K171547Qualisys Clinical SystemQualisys ABK173931MindMotion(TM) GOMindmaze SAK172882UINCARE HOMEUincare Corp.

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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