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FDA 510(k)

EasyWhip

K-Number: K210675 · 2021-05-03

ApplicantWinter Innovations, Inc.
Decision Date2021-05-03
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EasyWhip is a medical device manufactured by Winter Innovations, Inc.. It received FDA 510(k) clearance on 2021-05-03 under approval number K210675. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EasyWhip?

EasyWhip is a medical device that received FDA 510(k) clearance on 2021-05-03. It is manufactured by Winter Innovations, Inc.. The 510(k) number is K210675.

When was EasyWhip approved by the FDA?

EasyWhip received FDA 510(k) clearance on 2021-05-03, under approval number K210675.

What company makes EasyWhip?

EasyWhip is manufactured by Winter Innovations, Inc..

What is the FDA product code for EasyWhip?

The FDA product code for EasyWhip is GAT.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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