WHILL Model F
K-Number: K221438 · 2022-06-07
Device Summary
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. The listed applicant is Whill, Inc.. The 510(k) number is K221438.
When did WHILL Model F receive FDA 510(k) clearance?
WHILL Model F received FDA 510(k) clearance on 2022-06-07, under 510(k) number K221438.
Who is the listed applicant for WHILL Model F?
The FDA 510(k) record lists Whill, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHILL Model F?
The FDA product code for WHILL Model F is ITI.
Other records listing Whill, 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.
Related Devices (Code: ITI)
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.
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.