FDA 510(k)

Drug Relief v1

K-Number: K211971 · 2021-11-05

Decision Date2021-11-05

Product CodePZR

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Drug Relief v1 is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys, Inc.. It received FDA 510(k) clearance on 2021-11-05 under 510(k) number K211971. 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 v1?

Drug Relief v1 is a medical device that received FDA 510(k) clearance on 2021-11-05. The listed applicant is Dyansys, Inc.. The 510(k) number is K211971.

When did Drug Relief v1 receive FDA 510(k) clearance?

Drug Relief v1 received FDA 510(k) clearance on 2021-11-05, under 510(k) number K211971.

Who is the listed applicant for Drug Relief v1?

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 v1?

The FDA product code for Drug Relief v1 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 K202940First 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.K201873Sparrow Therapy SystemSpark Biomedical, Inc.K173861Drug ReliefDyansys, Inc.

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.