FDA 510(k)

EasyWhip Family

K-Number: K261021 · 2026-07-01

Decision Date2026-07-01

Product CodeGAT

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

EasyWhip Family is the device name listed in this FDA 510(k) record. The listed applicant is Winter Innovations, Inc.. It received FDA 510(k) clearance on 2026-07-01 under 510(k) number K261021. 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 Family?

EasyWhip Family is a medical device that received FDA 510(k) clearance on 2026-07-01. The listed applicant is Winter Innovations, Inc.. The 510(k) number is K261021.

When did EasyWhip Family receive FDA 510(k) clearance?

EasyWhip Family received FDA 510(k) clearance on 2026-07-01, under 510(k) number K261021.

Who is the listed applicant for EasyWhip Family?

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

What is the FDA product code for EasyWhip Family?

The FDA product code for EasyWhip Family is GAT.

Other records listing Winter Innovations, Inc. as applicant

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.

K210675EasyWhip

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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.