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FDA 510(k)

CERVICAL FUNCTION INDICATOR

K-Number: K943430 · 1995-03-13

ApplicantWhiplash Analysis, Inc.
Decision Date1995-03-13
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERVICAL FUNCTION INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Whiplash Analysis, Inc.. It received FDA 510(k) clearance on 1995-03-13 under 510(k) number K943430. 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 CERVICAL FUNCTION INDICATOR?

CERVICAL FUNCTION INDICATOR is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Whiplash Analysis, Inc.. The 510(k) number is K943430.

When did CERVICAL FUNCTION INDICATOR receive FDA 510(k) clearance?

CERVICAL FUNCTION INDICATOR received FDA 510(k) clearance on 1995-03-13, under 510(k) number K943430.

Who is the listed applicant for CERVICAL FUNCTION INDICATOR?

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

What is the FDA product code for CERVICAL FUNCTION INDICATOR?

The FDA product code for CERVICAL FUNCTION INDICATOR 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

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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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