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Precision TENS3900

FDA UDI

Class II (US FDA UDI)

by Medical Finance Resources Inc

Identity

Trade Name
Precision TENS3900 FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
PRECISION TENS3900 4 MODE 90mA ANALOG TENS UNIT WITH TIMER FDA UDI
Model / Reference
TENS3900V2-MFR FDA UDI
Description
PRECISION TENS3900 4 MODE 90mA ANALOG TENS UNIT WITH TIMER FDA UDI

Identifiers

Catalog Number
TENS3900V2-MFR FDA UDI
Primary DI / UDI-DI
00850209007016 FDA UDI
510(k) Number
K003487 FDA UDI
FDA Product Code
GZJ FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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: Physical therapy transcutaneous neuromuscular electrical stimulation system

Precision TENS3900 by Medical Finance Resources Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c15c6727-c3b0-42ad-9512-adeef849c6b4 35 fields · synced May 31, 2026