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FDA 510(k)

Bonine Acupressure Bands

K-Number: K211823 · 2021-09-01

ApplicantWellspring Pharmaceutical Corporation
Decision Date2021-09-01
Product CodeMVV
DecisionSubstantially Equivalent

Device Summary

Bonine Acupressure Bands is the device name listed in this FDA 510(k) record. The listed applicant is Wellspring Pharmaceutical Corporation. It received FDA 510(k) clearance on 2021-09-01 under 510(k) 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. The listed applicant is Wellspring Pharmaceutical Corporation. The 510(k) number is K211823.

When did Bonine Acupressure Bands receive FDA 510(k) clearance?

Bonine Acupressure Bands received FDA 510(k) clearance on 2021-09-01, under 510(k) number K211823.

Who is the listed applicant for Bonine Acupressure Bands?

The FDA 510(k) record lists Wellspring Pharmaceutical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bonine Acupressure Bands?

The FDA product code for Bonine Acupressure Bands is MVV.

Related Devices (Code: MVV)

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.

K220289FridaMom Anti-Nausea BandsFridababy, LLCK193374TumEase Acupressure BraceletsMumease

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.

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