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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Drug-delivery iontophoresis system electrode, active FDA UDI
Device Name
I-BRESIS, CONTROLLER FDA UDI
Model / Reference
1361 FDA UDI
Description
I-BRESIS, CONTROLLER FDA UDI

Identifiers

Primary DI / UDI-DI
00190446238188 FDA UDI
510(k) Number
K072946 FDA UDI
FDA Product Code
EGJ FDA UDI
GMDN Term
Drug-delivery iontophoresis system electrode, active FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5525 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

No

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: Drug-delivery iontophoresis system electrode, active

Chattanooga by Djo, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Drug-delivery iontophoresis system electrode, active.

Cleared under the same submission

K072946 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI a6e3cdcd-72a3-4bbd-a83e-b5881ee694e6 34 fields · synced May 30, 2026