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FDA 510(k)

WHILL Model C2

K-Number: K213383 · 2021-11-09

ApplicantWhill, Inc.
Decision Date2021-11-09
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHILL Model C2 is a medical device manufactured by Whill, Inc.. It received FDA 510(k) clearance on 2021-11-09 under approval number K213383. 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 C2?

WHILL Model C2 is a medical device that received FDA 510(k) clearance on 2021-11-09. It is manufactured by Whill, Inc.. The 510(k) number is K213383.

When was WHILL Model C2 approved by the FDA?

WHILL Model C2 received FDA 510(k) clearance on 2021-11-09, under approval number K213383.

What company makes WHILL Model C2?

WHILL Model C2 is manufactured by Whill, Inc..

What is the FDA product code for WHILL Model C2?

The FDA product code for WHILL Model C2 is ITI.

Other Devices by Whill, Inc.

K153543WHILL Model M K221438WHILL Model F 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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