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Liberator

FDA UDI

Class II (US FDA UDI)

by Caire Inc.

Identity

Trade Name
Liberator FDA UDI
Generic Name
Stationary liquid oxygen container FDA UDI
Device Name
Base Liquid Oxygen Respiratory Equipment, Top Fill, 15 LPM, 20 PSI FDA UDI
Model / Reference
13263686 FDA UDI
Description
Base Liquid Oxygen Respiratory Equipment, Top Fill, 15 LPM, 20 PSI FDA UDI

Identifiers

Primary DI / UDI-DI
M766132636860 FDA UDI
510(k) Number
K800742 FDA UDI
FDA Product Code
BYJ FDA UDI
GMDN Term
Stationary liquid oxygen container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5655 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stationary liquid oxygen container

Liberator by Caire Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary liquid oxygen container.

Cleared under the same submission

K800742 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caire Inc.

Sources (1)

  • FDA UDI ebc4388a-8349-4464-8176-9b44b43ba577 34 fields · synced Jun 8, 2026