← Back to catalogue

Equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Equate FDA UDI
Generic Name
Wart-removal cryogenic kit FDA UDI
Device Name
Equate Freeze Wart Remover 18 applications FDA UDI
Model / Reference
Wart Remover FDA UDI
Description
Equate Freeze Wart Remover 18 applications FDA UDI

Identifiers

Primary DI / UDI-DI
00194346121694 FDA UDI
510(k) Number
K210529 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Wart-removal cryogenic kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Wart-removal cryogenic kit

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

Similar devices

Also classified as Wart-removal cryogenic kit.

Cleared under the same submission

K210529 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 c32941bd-7ab5-44e4-9ed6-5e660195042b 35 fields · synced May 30, 2026