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Evolution

FDA UDI

Class II (US FDA UDI)

by Inovo, Inc.

Identity

Trade Name
EVOLUTION FDA UDI
Generic Name
Non-fixed medical gas cylinder regulator FDA UDI
Device Name
EVOLUTION ELECTRONIC OXYGEN CONSERVER FDA UDI
Model / Reference
OM-900CE FDA UDI
Description
EVOLUTION ELECTRONIC OXYGEN CONSERVER FDA UDI

Identifiers

Primary DI / UDI-DI
00822383018522 FDA UDI
510(k) Number
K103392 FDA UDI
FDA Product Code
NFB FDA UDI
GMDN Term
Non-fixed medical gas cylinder regulator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

No

FDA UDI

Category: Non-fixed medical gas cylinder regulator

Evolution by Inovo, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-fixed medical gas cylinder regulator.

Cleared under the same submission

K103392 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inovo, Inc.

Sources (1)

  • FDA UDI 43b7e123-eaab-4f2b-92e8-c41d549b79f8 34 fields · synced Jun 8, 2026