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FDA 510(k)

FRYE ADJUSTING INSTRUMENT

K-Number: K021238 · 2002-10-09

ApplicantFrye Health Systems
Decision Date2002-10-09
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

FRYE ADJUSTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Frye Health Systems. It received FDA 510(k) clearance on 2002-10-09 under 510(k) number K021238. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRYE ADJUSTING INSTRUMENT?

FRYE ADJUSTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Frye Health Systems. The 510(k) number is K021238.

When did FRYE ADJUSTING INSTRUMENT receive FDA 510(k) clearance?

FRYE ADJUSTING INSTRUMENT received FDA 510(k) clearance on 2002-10-09, under 510(k) number K021238.

Who is the listed applicant for FRYE ADJUSTING INSTRUMENT?

The FDA 510(k) record lists Frye Health Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRYE ADJUSTING INSTRUMENT?

The FDA product code for FRYE ADJUSTING INSTRUMENT is LXM.

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Related Devices (Code: LXM)

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.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

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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