Drug Relief v1
K-Number: K211971 · 2021-11-05
ApplicantDyansys, Inc.
Decision Date2021-11-05
Product CodePZR
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Drug Relief v1 is a medical device manufactured by Dyansys, Inc.. It received FDA 510(k) clearance on 2021-11-05 under approval 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. It is manufactured by Dyansys, Inc.. The 510(k) number is K211971.
When was Drug Relief v1 approved by the FDA?
Drug Relief v1 received FDA 510(k) clearance on 2021-11-05, under approval number K211971.
What company makes Drug Relief v1?
Drug Relief v1 is manufactured by Dyansys, Inc..
What is the FDA product code for Drug Relief v1?
The FDA product code for Drug Relief v1 is PZR.
Other Devices by Dyansys, Inc.
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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.