Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

StimSox(TM) System

K-Number: K171071 · 2017-08-09

ApplicantStimmed, LLC
Decision Date2017-08-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

StimSox(TM) System is a medical device manufactured by Stimmed, LLC. It received FDA 510(k) clearance on 2017-08-09 under approval number K171071. 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 StimSox(TM) System?

StimSox(TM) System is a medical device that received FDA 510(k) clearance on 2017-08-09. It is manufactured by Stimmed, LLC. The 510(k) number is K171071.

When was StimSox(TM) System approved by the FDA?

StimSox(TM) System received FDA 510(k) clearance on 2017-08-09, under approval number K171071.

What company makes StimSox(TM) System?

StimSox(TM) System is manufactured by Stimmed, LLC.

What is the FDA product code for StimSox(TM) System?

The FDA product code for StimSox(TM) System is IPF.

Other Devices by Stimmed, LLC

K151922StimSox(TM) System

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.

↑