Physiq
K-Number: K202079 · 2020-11-25
ApplicantEl.En Electronic Engineering Spa
Decision Date2020-11-25
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Physiq is a medical device manufactured by El.En Electronic Engineering Spa. It received FDA 510(k) clearance on 2020-11-25 under approval number K202079. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Physiq?
Physiq is a medical device that received FDA 510(k) clearance on 2020-11-25. It is manufactured by El.En Electronic Engineering Spa. The 510(k) number is K202079.
When was Physiq approved by the FDA?
Physiq received FDA 510(k) clearance on 2020-11-25, under approval number K202079.
What company makes Physiq?
Physiq is manufactured by El.En Electronic Engineering Spa.
What is the FDA product code for Physiq?
The FDA product code for Physiq is IPF.
Other Devices by El.En Electronic Engineering Spa
Related Devices (Code: IPF)
K160614Xcite Clinical StationRestorative Therapies, Inc.
K163067CyMedica e-vive System; CY-1000Cymedica Orthopedics, Inc.
K160992HPM-6000BTL Industries, Inc.
K151922StimSox(TM) SystemStimmed, LLC
K153696Chattanooga Revolution WirelessDjo, LLC
K160299geko(TM) Plus R-2 Neuromuscular StimulatorFirstkind Limited
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.