Identity
- Trade Name
- InterX FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- The InterX® 900 Single Patient Systems are the latest addition to the InterX family and have been designed with ease of use in mind. The same unique InterX Neurostimulation is delivered through self-adhesive disposable dual electrodes and through body specific conductive garments which are attached to relevant parts of the body. Built in preset stimulation patterns deliver a range of high and low frequency stimulation to optimize the effects of treatment and assist the patient in returning to full function. FDA UDI
- Model / Reference
- 900 FDA UDI
- Description
- The InterX® 900 Single Patient Systems are the latest addition to the InterX family and have been designed with ease of use in mind. The same unique InterX Neurostimulation is delivered through self-adhesive disposable dual electrodes and through body specific conductive garments which are attached to relevant parts of the body. Built in preset stimulation patterns deliver a range of high and low frequency stimulation to optimize the effects of treatment and assist the patient in returning to full function. FDA UDI
Identifiers
- Catalog Number
- 1478-001 FDA UDI
- Primary DI / UDI-DI
- 00851894007046 FDA UDI
- 510(k) Number
- K042912 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
Dimensions & Sizes
- Size
- Weight — 185 Gram FDA UDIHeight — 43 Millimeter FDA UDIWidth — 52 Millimeter FDA UDILength — 215 Millimeter FDA UDI
Category: Physical therapy transcutaneous neuromuscular electrical stimulation system
InterX by Htk Enterprises, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K042912 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Htk Enterprises, Inc.
Sources (1)
- FDA UDI fca16d46-a27e-434a-af13-cae7198ec43c 38 fields · synced May 30, 2026