AWQ-104L ED3923

GUDID 14897076720016

The AWQ-104L w L-Digital Meter is the latest improved version of the multipurpose WQ-10 electro-therapy series from China, now with 4 outputs and large 0.5" x 0.9" LCD digital meter. The AWQ-104L is able to display and fine tune frequency selection through two separate ranges: 1 to 100 Hz (low) and 10 to 1,000 Hz (High). Unit also features: 4 independently controlled output channels which provide stimulation to 8 needles, polarity reversal [i.e. tonification (+) and sedation (-)] switches for each channel, Hi/Low voltage switch, and 2 frequency ranges (X1, X10). New integrated circuitry assures no interference or crossover. The AWQ-104L is also capable of delivering micro-current when the intensity is set just below the sensorial threshold level. Powered by 9 volt battery. Three adjustable pulse modes are also offered: continuous, intermittent (discontinuous), and dense-disperse. Accessories include 5" long pen shaped treatment probe with hand ground pole and wire, 4 sets of alligator clip wires, sturdy carrying case, 9-volt battery, and instructions. 1-year warranty from date of purchase.

TENS PLUS INDUSTRIAL COMPANY

Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 14897076720016
• NIH Device Record Key: a45fca27-17d6-42fc-8443-e1aa05bf84fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AWQ-104L
• Version Model Number: ED3923
• Catalog Number: ED3923
• Company DUNS: 663211978
• Company Name: TENS PLUS INDUSTRIAL COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-722-8775
• Email: customerservice@lhasaoms.com
• Phone: 800-722-8775
• Email: customerservice@lhasaoms.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	14897076720016 [Primary]
GS1	34897076720010 [Package]; Package: Master Case [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050989

FDA Product Code

• GZJ: Stimulator, Nerve, Transcutaneous, For Pain Relief

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-08-04

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