FDA 510(k)

Drug Relief

K-Number: K173861 · 2018-05-02

Decision Date2018-05-02

Product CodePZR

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Drug Relief is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys, Inc.. It received FDA 510(k) clearance on 2018-05-02 under 510(k) number K173861. The device is classified under product code PZR. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Drug Relief?

Drug Relief is a medical device that received FDA 510(k) clearance on 2018-05-02. The listed applicant is Dyansys, Inc.. The 510(k) number is K173861.

When did Drug Relief receive FDA 510(k) clearance?

Drug Relief received FDA 510(k) clearance on 2018-05-02, under 510(k) number K173861.

Who is the listed applicant for Drug Relief?

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

What is the FDA product code for Drug Relief?

The FDA product code for Drug Relief is PZR.

Other records listing Dyansys, Inc. as applicant

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.

K221425Primary Relief K221231Drug Relief v1 K220397ANSiStim-PP K213188Primary Relief K212859First Relief K211971Drug Relief v1

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Related Devices (Code: PZR)

K251246Sparrow AscentSpark Biomedical, Inc.K233166NET Recovery Corp/NET DeviceNet Recovery K230796Sparrow AscentSpark Biomedical, Inc.K221231Drug Relief v1Dyansys, Inc.K211971Drug Relief v1Dyansys, Inc.K201873Sparrow Therapy SystemSpark Biomedical, Inc.

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.