Vicks

FDA UDI

Class II (US FDA UDI)

by Kaz Usa, Inc.

Identity

Trade Name: Vicks FDA UDI
Generic Name: Intermittent electronic patient thermometer FDA UDI
Device Name: Thermometer, 15 sec, Digital, Audio Fever Signal FDA UDI
Model / Reference: V901USV1 FDA UDI
Description: Thermometer, 15 sec, Digital, Audio Fever Signal FDA UDI

Identifiers

Primary DI / UDI-DI: 00328785000269 FDA UDI
510(k) Number: K851146 FDA UDI
FDA Product Code: FLL FDA UDI
GMDN Term: Intermittent electronic patient thermometer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.2910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Intermittent electronic patient thermometer

Vicks by Kaz Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K851146 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Kaz Usa, Inc.

Sources (1)

FDA UDI d7dc5c88-2e10-4ca0-a09d-f8f7a911218e 35 fields · synced Jun 8, 2026