Physiq

Stimulator, Muscle, Powered

El. En. Electronic Engineering SPA

The following data is part of a premarket notification filed by El. En. Electronic Engineering Spa with the FDA for Physiq.

Pre-market Notification Details

• Device ID: K202079
• 510k Number: K202079
• Device Name: Physiq
• Classification: Stimulator, Muscle, Powered
• Applicant: El. En. Electronic Engineering SPA Via Baldanzese 17 Calenzano, IT 50041
• Contact: Paolo Peruzzi
• Correspondent: Paolo Peruzzi; El. En. Electronic Engineering SPA Via Baldanzese 17 Calenzano, IT 50041
• Product Code: IPF
• CFR Regulation Number: 890.5850 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2020-07-27
• Decision Date: 2020-11-25

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
08057017760535	K202079	000