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FDA 510(k)

MEDX CERVICAL EXTENSION TEST & REHAB MACHINE

K-Number: K896553 · 1990-01-02

ApplicantMedx Corp.
Decision Date1990-01-02
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDX CERVICAL EXTENSION TEST & REHAB MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Medx Corp.. It received FDA 510(k) clearance on 1990-01-02 under 510(k) number K896553. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDX CERVICAL EXTENSION TEST & REHAB MACHINE?

MEDX CERVICAL EXTENSION TEST & REHAB MACHINE is a medical device that received FDA 510(k) clearance on 1990-01-02. The listed applicant is Medx Corp.. The 510(k) number is K896553.

When did MEDX CERVICAL EXTENSION TEST & REHAB MACHINE receive FDA 510(k) clearance?

MEDX CERVICAL EXTENSION TEST & REHAB MACHINE received FDA 510(k) clearance on 1990-01-02, under 510(k) number K896553.

Who is the listed applicant for MEDX CERVICAL EXTENSION TEST & REHAB MACHINE?

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

What is the FDA product code for MEDX CERVICAL EXTENSION TEST & REHAB MACHINE?

The FDA product code for MEDX CERVICAL EXTENSION TEST & REHAB MACHINE is IKK.

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.

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Other records listing Medx Corp. 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.

K911666MEDX MACHINEK895236MEDX REHABILITATION MACHINE

Related Devices (Code: IKK)

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.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

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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