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Coda®

FDA UDI

Class II (US FDA UDI)

by LifeGlobal Group, LLC

Identity

Trade Name
Coda® FDA UDI
Generic Name
Non-respiratory device ambient air filter FDA UDI
Device Name
Coda Lo-Boy Quarterly kit, 1st, 2nd, 3rd Stage FDA UDI
Model / Reference
GXTQ-042 FDA UDI
Description
Coda Lo-Boy Quarterly kit, 1st, 2nd, 3rd Stage FDA UDI

Identifiers

Catalog Number
GXTQ-042 FDA UDI
Primary DI / UDI-DI
00815965021720 FDA UDI
510(k) Number
K001486 FDA UDI
FDA Product Code
MQG FDA UDI
GMDN Term
Non-respiratory device ambient air filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6120 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

Yes

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

No

FDA UDI

Category: Non-respiratory device ambient air filter

Coda® by LifeGlobal Group, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-respiratory device ambient air filter.

Cleared under the same submission

K001486 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LifeGlobal Group, LLC

Sources (1)

  • FDA UDI b7d0630a-08c7-4095-9532-4564156f0107 36 fields · synced Jun 9, 2026