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equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
equate FDA UDI
Generic Name
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
Equate Covid-19 Test Kit Single FDA UDI
Model / Reference
ICO-3000 FDA UDI
Description
Equate Covid-19 Test Kit Single FDA UDI

Identifiers

Primary DI / UDI-DI
06930251802365 FDA UDI
510(k) Number
K233842 FDA UDI
FDA Product Code
QYT FDA UDI
GMDN Term
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3984 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

equate by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing.

Cleared under the same submission

K233842 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 9c8e4d7c-35bb-4674-b00b-41d1a78506dc 34 fields · synced May 30, 2026