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: K131290
• 510k Number: K131290
• Device Name: IQ TECHNOLOGIES
• Classification: Stimulator, Nerve, Transcutaneous, Over-the-counter
• Applicant: IQ TECHNOLOGIES INC. 1631 E. Sunset Road Suite C 103 Las Vegas, NV 89119
• Contact: Eli Josef
• Correspondent: Eli Josef; IQ TECHNOLOGIES INC. 1631 E. Sunset Road Suite C 103 Las Vegas, NV 89119
• Product Code: NUH
• CFR Regulation Number: 882.5890 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2013-05-06
• Decision Date: 2014-08-06
• Summary: summary