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FDA 510(k)

JTECH ADJUSTER REFLEX GUN

K-Number: K974376 · 1998-02-18

ApplicantJ-Tech Medical, Inc.
Decision Date1998-02-18
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

JTECH ADJUSTER REFLEX GUN is the device name listed in this FDA 510(k) record. The listed applicant is J-Tech Medical, Inc.. It received FDA 510(k) clearance on 1998-02-18 under 510(k) number K974376. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JTECH ADJUSTER REFLEX GUN?

JTECH ADJUSTER REFLEX GUN is a medical device that received FDA 510(k) clearance on 1998-02-18. The listed applicant is J-Tech Medical, Inc.. The 510(k) number is K974376.

When did JTECH ADJUSTER REFLEX GUN receive FDA 510(k) clearance?

JTECH ADJUSTER REFLEX GUN received FDA 510(k) clearance on 1998-02-18, under 510(k) number K974376.

Who is the listed applicant for JTECH ADJUSTER REFLEX GUN?

The FDA 510(k) record lists J-Tech Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JTECH ADJUSTER REFLEX GUN?

The FDA product code for JTECH ADJUSTER REFLEX GUN is LXM.

Related Clinical Trials

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Other records listing J-Tech Medical, 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.

K971407JTECH COMMANDER AND ALGOMETER

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

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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