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FrostAway™

FDA UDI

Class II (US FDA UDI)

by H & O Equipments SA

Identity

Trade Name
FrostAway™ FDA UDI
Generic Name
General cryosurgical system, cryogen gas, mechanical FDA UDI
Model / Reference
FrostAway Pen cartridges FDA UDI

Identifiers

Catalog Number
FROSTAWAYPEN-CA FDA UDI
Primary DI / UDI-DI
15407008487017 FDA UDI
510(k) Number
K024009 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
General cryosurgical system, cryogen gas, mechanical 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General cryosurgical system, cryogen gas, mechanicalNitrous oxide gas cartridge

FrostAway™ by H & O Equipments SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitrous oxide gas cartridge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
H & O Equipments SA

Sources (1)

  • FDA UDI 60d7f170-c405-440a-9c41-3f43b85bf465 35 fields · synced Jun 8, 2026