IQ Technologies

Stimulator, Nerve, Transcutaneous, Over-the-counter

IQ Technologies Inc.

The following data is part of a premarket notification filed by Iq Technologies Inc. with the FDA for Iq Technologies.

Pre-market Notification Details

• Device ID: K170659
• 510k Number: K170659
• Device Name: IQ Technologies
• Classification: Stimulator, Nerve, Transcutaneous, Over-the-counter
• Applicant: IQ Technologies Inc. 6672 Spencer St., Ste 800 Las Vegas, NV 89119
• Contact: Elli Josef
• Correspondent: Bill Quanqin Dai; Dr Certification LLC 1142 S. Diamond Bar Blvd, #861 Diamond Bar, CA 91765
• Product Code: NUH
• CFR Regulation Number: 882.5890 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2017-03-03
• Decision Date: 2017-05-26
• Summary: summary