ANKLE REFLEX TREATMENT UNIT (ARTU)— 510(k) K873658

Name: FDA 510(k) clearance K873658
Creator: U.S. Food and Drug Administration
Published: 1988-04-21

Substantially Equivalent

Universal Gym Equipment, Inc.

FDA 510(k) clearance K873658 for ANKLE REFLEX TREATMENT UNIT (ARTU), Substantially Equivalent on 1988-04-21. Applicant: Universal Gym Equipment, Inc.. Device class: 1.

Clearance details

Applicant: Universal Gym Equipment, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1987-09-10
Decision date: 1988-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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