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FDA 510(k)

APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE

K-Number: K952683 · 1997-04-01

ApplicantWholesale Medical Imports, Inc.
Decision Date1997-04-01
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Wholesale Medical Imports, Inc.. It received FDA 510(k) clearance on 1997-04-01 under 510(k) number K952683. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE?

APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE is a medical device that received FDA 510(k) clearance on 1997-04-01. The listed applicant is Wholesale Medical Imports, Inc.. The 510(k) number is K952683.

When did APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE receive FDA 510(k) clearance?

APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE received FDA 510(k) clearance on 1997-04-01, under 510(k) number K952683.

Who is the listed applicant for APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE?

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

What is the FDA product code for APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE?

The FDA product code for APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE is LIH.

Related Clinical Trials

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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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