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FDA 510(k)

WatchMate Software

K-Number: K260300 · 2026-06-15

ApplicantAnumana, Inc.
Decision Date2026-06-15
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WatchMate Software is the device name listed in this FDA 510(k) record. The listed applicant is Anumana, Inc.. It received FDA 510(k) clearance on 2026-06-15 under 510(k) number K260300. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WatchMate Software?

WatchMate Software is a medical device that received FDA 510(k) clearance on 2026-06-15. The listed applicant is Anumana, Inc.. The 510(k) number is K260300.

When did WatchMate Software receive FDA 510(k) clearance?

WatchMate Software received FDA 510(k) clearance on 2026-06-15, under 510(k) number K260300.

Who is the listed applicant for WatchMate Software?

The FDA 510(k) record lists Anumana, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WatchMate Software?

The FDA product code for WatchMate Software is QIH.

Other records listing Anumana, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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