APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE— 510(k) K952683

Name: FDA 510(k) clearance K952683
Creator: U.S. Food and Drug Administration
Published: 1997-04-01

Substantially Equivalent

Wholesale Medical Imports, Inc.

FDA 510(k) clearance K952683 for APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE, Substantially Equivalent on 1997-04-01. Applicant: Wholesale Medical Imports, Inc.. Device class: 2.

Clearance details

Applicant: Wholesale Medical Imports, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1995-06-12
Decision date: 1997-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck,, NY, US

Download summary PDF View on FDA.gov ↗

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