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FDA 510(k)

Digitimer DS7AP Constant Current Stimulator

K-Number: K172381 · 2018-03-06

ApplicantDigitimer , Ltd.
Decision Date2018-03-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Digitimer DS7AP Constant Current Stimulator is a medical device manufactured by Digitimer , Ltd.. It received FDA 510(k) clearance on 2018-03-06 under approval number K172381. 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 Digitimer DS7AP Constant Current Stimulator?

Digitimer DS7AP Constant Current Stimulator is a medical device that received FDA 510(k) clearance on 2018-03-06. It is manufactured by Digitimer , Ltd.. The 510(k) number is K172381.

When was Digitimer DS7AP Constant Current Stimulator approved by the FDA?

Digitimer DS7AP Constant Current Stimulator received FDA 510(k) clearance on 2018-03-06, under approval number K172381.

What company makes Digitimer DS7AP Constant Current Stimulator?

Digitimer DS7AP Constant Current Stimulator is manufactured by Digitimer , Ltd..

What is the FDA product code for Digitimer DS7AP Constant Current Stimulator?

The FDA product code for Digitimer DS7AP Constant Current Stimulator is IPF.

Related Clinical Trials

NCT07187388 Investigating the Impact of Electrical Stimulation on Facial Pain, Jaw Movement and Oral Health in People With Motor Neuron Disease. RECRUITING NCT00453505 Modulation of Motor Function by Stimulation of the Central and Peripheral Nervous System COMPLETED NCT04986293 CPAP or BiPAP for Motion Mitigation During Radiotherapy RECRUITING NCT07531238 Transcranial Temporal Interference Stimulation (tTIS) To Modulate Essential Tremor NOT_YET_RECRUITING NCT07354139 Using Non-invasive Brain Stimulation to Explore Potential Treatments to Reduce Speech Errors in Adults Who Stutter RECRUITING NCT03651648 Apnea Treatment in Premature Infants Using an Automatic Vibro-tactile Stimulator Triggered by the Detection of Apnea-bradycardia. COMPLETED

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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