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FDA 510(k)

WHILL Model F

K-Number: K221438 · 2022-06-07

ApplicantWhill, Inc.
Decision Date2022-06-07
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHILL Model F is a medical device manufactured by Whill, Inc.. It received FDA 510(k) clearance on 2022-06-07 under approval number K221438. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHILL Model F?

WHILL Model F is a medical device that received FDA 510(k) clearance on 2022-06-07. It is manufactured by Whill, Inc.. The 510(k) number is K221438.

When was WHILL Model F approved by the FDA?

WHILL Model F received FDA 510(k) clearance on 2022-06-07, under approval number K221438.

What company makes WHILL Model F?

WHILL Model F is manufactured by Whill, Inc..

What is the FDA product code for WHILL Model F?

The FDA product code for WHILL Model F is ITI.

Other Devices by Whill, Inc.

K153543WHILL Model M K213383WHILL Model C2 K242760WHILL Model R

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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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