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FDA 510(k)

Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test

K-Number: K260754 · 2026-06-05

ApplicantAssure Tech., LLC
Decision Date2026-06-05
Product CodeQYT
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test is the device name listed in this FDA 510(k) record. The listed applicant is Assure Tech., LLC. It received FDA 510(k) clearance on 2026-06-05 under 510(k) number K260754. The device is classified under product code QYT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test?

Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test is a medical device that received FDA 510(k) clearance on 2026-06-05. The listed applicant is Assure Tech., LLC. The 510(k) number is K260754.

When did Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test receive FDA 510(k) clearance?

Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test received FDA 510(k) clearance on 2026-06-05, under 510(k) number K260754.

Who is the listed applicant for Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test?

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

What is the FDA product code for Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test?

The FDA product code for Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test is QYT.

Other records listing Assure Tech., LLC as applicant

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Related Devices (Code: QYT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260095Heal-Check Rapid COVID-19 Antigen Self-TestHealgen Scientific,, LLCK251916GenBody COVID-19 Ag Home TestGenbody.Inc.K251595COVID-19 Detect Rapid Self -TestInBios International, Inc.K251753GenaCheck COVID-19 Rapid Self-TestGenabio Diagnostics, Inc.K241313OHC COVID-19 Antigen Self TestOsang, LLCK243518BinaxNOW™ COVID-19 Antigen Self TestAbbott Diagnostics Scarborough, Inc.

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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