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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 the device name listed in this FDA 510(k) record. The listed applicant is Digitimer , Ltd.. It received FDA 510(k) clearance on 2018-03-06 under 510(k) 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. The listed applicant is Digitimer , Ltd.. The 510(k) number is K172381.

When did Digitimer DS7AP Constant Current Stimulator receive FDA 510(k) clearance?

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

Who is the listed applicant for Digitimer DS7AP Constant Current Stimulator?

The FDA 510(k) record lists Digitimer , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07531238Transcranial Temporal Interference Stimulation (tTIS) To Modulate Essential TremorNOT_YET_RECRUITING

Related Devices (Code: IPF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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