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FDA 510(k)

TumEase Acupressure Bracelets

K-Number: K193374 · 2020-03-04

ApplicantMumease
Decision Date2020-03-04
Product CodeMVV
DecisionSubstantially Equivalent

Device Summary

TumEase Acupressure Bracelets is the device name listed in this FDA 510(k) record. The listed applicant is Mumease. It received FDA 510(k) clearance on 2020-03-04 under 510(k) number K193374. The device is classified under product code MVV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TumEase Acupressure Bracelets?

TumEase Acupressure Bracelets is a medical device that received FDA 510(k) clearance on 2020-03-04. The listed applicant is Mumease. The 510(k) number is K193374.

When did TumEase Acupressure Bracelets receive FDA 510(k) clearance?

TumEase Acupressure Bracelets received FDA 510(k) clearance on 2020-03-04, under 510(k) number K193374.

Who is the listed applicant for TumEase Acupressure Bracelets?

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

What is the FDA product code for TumEase Acupressure Bracelets?

The FDA product code for TumEase Acupressure Bracelets 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, LLCK211823Bonine Acupressure BandsWellspring Pharmaceutical Corporation

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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