Pocket Neb

FDA UDI

Class II (US FDA UDI)

by MicroVapor Devices, LLC

Identity

Trade Name: Pocket Neb FDA UDI
Generic Name: Ultrasonic nebulizing system FDA UDI
Device Name: The MVD-70, Pocket Neb is an electronic vibrating mesh nebulizer designed to aerosolize liquid medications for inhalation by the patient. The device may be used with pediatric and adult patients in and out of the home environment. FDA UDI
Model / Reference: MVD-70 FDA UDI
Description: The MVD-70, Pocket Neb is an electronic vibrating mesh nebulizer designed to aerosolize liquid medications for inhalation by the patient. The device may be used with pediatric and adult patients in and out of the home environment. FDA UDI

Identifiers

Primary DI / UDI-DI: 00856702006013 FDA UDI
510(k) Number: K142541 FDA UDI
FDA Product Code: CAF FDA UDI
GMDN Term: Ultrasonic nebulizing system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5630 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Ultrasonic nebulizing system

Pocket Neb by MicroVapor Devices, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K142541 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: MicroVapor Devices, LLC

Sources (1)

FDA UDI b65011a9-065a-48bd-bd39-4343ee118d23 34 fields · synced Jun 1, 2026