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FDA 510(k)

WHILL Model M

K-Number: K153543 · 2016-02-12

ApplicantWhill, Inc.
Decision Date2016-02-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHILL Model M is a medical device manufactured by Whill, Inc.. It received FDA 510(k) clearance on 2016-02-12 under approval number K153543. 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 M?

WHILL Model M is a medical device that received FDA 510(k) clearance on 2016-02-12. It is manufactured by Whill, Inc.. The 510(k) number is K153543.

When was WHILL Model M approved by the FDA?

WHILL Model M received FDA 510(k) clearance on 2016-02-12, under approval number K153543.

What company makes WHILL Model M?

WHILL Model M is manufactured by Whill, Inc..

What is the FDA product code for WHILL Model M?

The FDA product code for WHILL Model M is ITI.

Other Devices by Whill, Inc.

K213383WHILL Model C2 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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