Identity
- Trade Name
- Neuroprobe 500 Pro FDA UDI
- Generic Name
- Multi-modality physical therapy system, professional-use FDA UDI
- Device Name
- The Neuroprobe® 500 Pro gives the clinician the option of using any combination of an Estim probe, Interferential Current in bipolar or quadripolar modes, or Monochromatic Infrared Therapy to reduce pain and increase circulation. Flexible neoprene pads deliver heat and Infrared therapy through multiple clusters of infrared and red visible super luminous diodes (SLD). The Neuroprobe® 500 Pro’s optional probe with fully adjustable parameters provides a wide variety of uses for pain management with trigger point stimulation for pain control. The Neuroprobe® 500 Pro provides a nerve block mode through treatment pads with high output capable of sensory nerve block, or through the optional probe to produce local trigger point anesthesia. FDA UDI
- Model / Reference
- 140500B FDA UDI
- Description
- The Neuroprobe® 500 Pro gives the clinician the option of using any combination of an Estim probe, Interferential Current in bipolar or quadripolar modes, or Monochromatic Infrared Therapy to reduce pain and increase circulation. Flexible neoprene pads deliver heat and Infrared therapy through multiple clusters of infrared and red visible super luminous diodes (SLD). The Neuroprobe® 500 Pro’s optional probe with fully adjustable parameters provides a wide variety of uses for pain management with trigger point stimulation for pain control. The Neuroprobe® 500 Pro provides a nerve block mode through treatment pads with high output capable of sensory nerve block, or through the optional probe to produce local trigger point anesthesia. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858703006054 FDA UDI
- 510(k) Number
- K831147 FDA UDI
- FDA Product Code
- GZJ FDA UDI
- GMDN Term
- Multi-modality physical therapy system, professional-use 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
Yes
FDA UDI
Category: Multi-modality physical therapy system, professional-use
Neuroprobe 500 Pro by Accelerated Care Plus Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multi-modality physical therapy system, professional-use.
- Dynatron 25 Series 525B — Dynatronics Corp. · Class II
- Dynatron Solaris Plus 708 — Dynatronics Corp. · Class II
- RAYJU — Hunan Ruijiu Technology Co., Ltd. · Class II
- WINBACK — WINBACK GO EAST · Class II
- BlueOnyx Pro — Tama Research Corporation · Class II
- silverfox — Silver Fox Corporation Limited · Class I
- STAR — ELETTRONICA PAGANI SRL · Class I
- silverfox — Silver Fox Corporation Limited · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Accelerated Care Plus Corp.
Sources (1)
- FDA UDI aceb953d-1d89-4577-9e57-25e86ed07747 35 fields · synced Jun 1, 2026