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FDA 510(k)

FridaMom Anti-Nausea Bands

K-Number: K220289 · 2022-06-29

ApplicantFridababy, LLC
Decision Date2022-06-29
Product CodeMVV
DecisionSubstantially Equivalent

Device Summary

FridaMom Anti-Nausea Bands is the device name listed in this FDA 510(k) record. The listed applicant is Fridababy, LLC. It received FDA 510(k) clearance on 2022-06-29 under 510(k) number K220289. The device is classified under product code MVV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FridaMom Anti-Nausea Bands?

FridaMom Anti-Nausea Bands is a medical device that received FDA 510(k) clearance on 2022-06-29. The listed applicant is Fridababy, LLC. The 510(k) number is K220289.

When did FridaMom Anti-Nausea Bands receive FDA 510(k) clearance?

FridaMom Anti-Nausea Bands received FDA 510(k) clearance on 2022-06-29, under 510(k) number K220289.

Who is the listed applicant for FridaMom Anti-Nausea Bands?

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

What is the FDA product code for FridaMom Anti-Nausea Bands?

The FDA product code for FridaMom Anti-Nausea 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.

K211823Bonine Acupressure BandsWellspring Pharmaceutical CorporationK193374TumEase 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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