Bonine Acupressure Bands
K-Number: K211823 · 2021-09-01
Decision Date2021-09-01
Product CodeMVV
DecisionSubstantially Equivalent
Device Summary
Bonine Acupressure Bands is a medical device manufactured by Wellspring Pharmaceutical Corporation. It received FDA 510(k) clearance on 2021-09-01 under approval number K211823. The device is classified under product code MVV. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bonine Acupressure Bands?
Bonine Acupressure Bands is a medical device that received FDA 510(k) clearance on 2021-09-01. It is manufactured by Wellspring Pharmaceutical Corporation. The 510(k) number is K211823.
When was Bonine Acupressure Bands approved by the FDA?
Bonine Acupressure Bands received FDA 510(k) clearance on 2021-09-01, under approval number K211823.
What company makes Bonine Acupressure Bands?
Bonine Acupressure Bands is manufactured by Wellspring Pharmaceutical Corporation.
What is the FDA product code for Bonine Acupressure Bands?
The FDA product code for Bonine Acupressure Bands is MVV.
Related Devices (Code: MVV)
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.