← Back to catalogue

Equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Equate FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
Equate Digital + Visual (analog) Pregnancy Test 2CT, 6DAY (compare to Clearblue) FDA UDI
Model / Reference
677296456 FDA UDI
Description
Equate Digital + Visual (analog) Pregnancy Test 2CT, 6DAY (compare to Clearblue) FDA UDI

Identifiers

Primary DI / UDI-DI
00194346473625 FDA UDI
510(k) Number
K172257 FDA UDI
K182328 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, self-testing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 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

Yes

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Category: Total human chorionic gonadotropin 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 Total human chorionic gonadotropin IVD, kit, rapid ICT, self-testing.

Cleared under the same submission

K182328 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 6d4a8e1f-b64e-4674-b7f8-f756bdd69488 34 fields · synced May 30, 2026