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FDA 510(k)

iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro

K-Number: K251085 · 2025-12-12

Decision Date2025-12-12
Product CodeSCA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro is a medical device manufactured by Ihealth Labs, Inc.. It received FDA 510(k) clearance on 2025-12-12 under approval number K251085. The device is classified under product code SCA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro?

iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro is a medical device that received FDA 510(k) clearance on 2025-12-12. It is manufactured by Ihealth Labs, Inc.. The 510(k) number is K251085.

When was iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro approved by the FDA?

iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro received FDA 510(k) clearance on 2025-12-12, under approval number K251085.

What company makes iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro?

iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro is manufactured by Ihealth Labs, Inc..

What is the FDA product code for iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro?

The FDA product code for iHealth Flu A&B/COVID-19/RSV Rapid Test; iHealth Flu A&B/COVID-19/RSV Rapid Test Pro is SCA.

Other Devices by Ihealth Labs, Inc.

Related Devices (Code: SCA)

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.