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FDA 510(k)

WHILL Model R

K-Number: K242760 · 2025-01-06

ApplicantWhill, Inc.
Decision Date2025-01-06
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHILL Model R is a medical device manufactured by Whill, Inc.. It received FDA 510(k) clearance on 2025-01-06 under approval number K242760. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHILL Model R?

WHILL Model R is a medical device that received FDA 510(k) clearance on 2025-01-06. It is manufactured by Whill, Inc.. The 510(k) number is K242760.

When was WHILL Model R approved by the FDA?

WHILL Model R received FDA 510(k) clearance on 2025-01-06, under approval number K242760.

What company makes WHILL Model R?

WHILL Model R is manufactured by Whill, Inc..

What is the FDA product code for WHILL Model R?

The FDA product code for WHILL Model R is INI.

Other Devices by Whill, Inc.

K153543WHILL Model M K213383WHILL Model C2 K221438WHILL Model F

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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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