MEDX CERVICAL EXTENSION TEST & REHAB MACHINE— 510(k) K896553

Name: FDA 510(k) clearance K896553
Creator: U.S. Food and Drug Administration
Published: 1990-01-02

Substantially Equivalent

Medx Corp.

FDA 510(k) clearance K896553 for MEDX CERVICAL EXTENSION TEST & REHAB MACHINE, Substantially Equivalent on 1990-01-02. Applicant: Medx Corp.. Device class: 2.

Clearance details

Applicant: Medx Corp.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1989-11-17
Decision date: 1990-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ocala, FL, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K896553

K-number listed on FDA's recall record

Z-0936-2015 — Cervical Extension Machine for Physical TherapyClass II·Terminated·MedX Holdings, Inc.·20131203

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K896553.

Data sourced from openFDA. This site is unofficial and independent of the FDA.