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RS-FBG Full Back Garment

FDA UDI

Class II (US FDA UDI)

by Rs Medical

Identity

Trade Name
RS-FBG Full Back Garment FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
RS-FBG Full Back Garment System, RS-4i Plus Pin Cable Set and treatment electrodes FDA UDI
Model / Reference
959-0050-00 FDA UDI
Description
RS-FBG Full Back Garment System, RS-4i Plus Pin Cable Set and treatment electrodes FDA UDI

Identifiers

Primary DI / UDI-DI
00850814007036 FDA UDI
510(k) Number
K090951 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Transcutaneous electrical stimulation electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transcutaneous electrical stimulation electrode, single-use

RS-FBG Full Back Garment by Rs Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation electrode, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rs Medical

Sources (1)

  • FDA UDI d5a604c5-9d2c-4917-b905-34a626f729e2 35 fields · synced May 30, 2026