Pro-Tech Jq-5C-S
Pro-Tech Jq-5C-S is a medical device (FDA Class II) made by Hi-Dow International Inc., cleared under FDA 510(k) K102598 on 13 May 2011 and listed in FDA GUDID since 25 Nov 2016 (UDI-DI 00851640007214), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00851640007214 | Date25 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK102598 | Date13 May 2011 | StatusActive |
Official records
- AccessGUDID record 00851640007214
- FDA 510(k) database K102598
Across registries
- FDA 510(k) K102598 decided 13 May 2011 Active
- FDA GUDID UDI-DI 00851640007214 listed 25 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K102598
- Listed FDA GUDID 00851640007214
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Pro-Tech
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / reference
- JQ-5C-S
- Primary DI / UDI-DI
- 00851640007214
- 510(k) Number
- FDA product code
- NUH, NGX
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 882.5890, 890.5850
- GUDID distribution status
- In Commercial Distribution
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