Drug Relief v1
K-Number: K221231 · 2022-06-06
ApplicantDyansys, Inc.
Decision Date2022-06-06
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 2022-06-06 under approval number K221231. 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 2022-06-06. It is manufactured by Dyansys, Inc.. The 510(k) number is K221231.
When was Drug Relief v1 approved by the FDA?
Drug Relief v1 received FDA 510(k) clearance on 2022-06-06, under approval number K221231.
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.
Related Devices (Code: PZR)
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.