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)

Drug Relief

K-Number: K173861 · 2018-05-02

ApplicantDyansys, Inc.
Decision Date2018-05-02
Product CodePZR
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Drug Relief is a medical device manufactured by Dyansys, Inc.. It received FDA 510(k) clearance on 2018-05-02 under approval 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. It is manufactured by Dyansys, Inc.. The 510(k) number is K173861.

When was Drug Relief approved by the FDA?

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

What company makes Drug Relief?

Drug Relief is manufactured by Dyansys, Inc..

What is the FDA product code for Drug Relief?

The FDA product code for Drug Relief is PZR.

Other Devices by Dyansys, Inc.

K170391ANSiStim-PP K202940First Relief v1 K212859First Relief K211971Drug Relief v1 K221425Primary Relief K221231Drug Relief v1

View all 9 devices →

Related Devices (Code: PZR)

DEN170018NSS-2 SystemInnovative Health Solutions (Ihs), Inc. K211971Drug Relief v1Dyansys, Inc. K201873Sparrow Therapy SystemSpark Biomedical, Inc. K221231Drug Relief v1Dyansys, Inc. K230796Sparrow AscentSpark Biomedical, Inc. K233166NET Recovery Corp/NET DeviceNet Recovery

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.

↑