Cathay CM5050FB
Cathay CM5050FB is a Class II device made by Cathay Manufacturing Corp., cleared under FDA 510(k) K020735 on 12 Jul 2002 and listed in FDA GUDID since 17 Apr 2017 (UDI-DI 06959006302226), 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 | Number06959006302226 | Date17 Apr 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020735 | Date12 Jul 2002 | StatusActive |
Official records
- AccessGUDID record 06959006302226
- FDA 510(k) database K020735
Across registries
- FDA 510(k) K020735 decided 12 Jul 2002 Active
- FDA GUDID UDI-DI 06959006302226 listed 17 Apr 2017 Listed
Timeline
- Cleared FDA 510(k) K020735
- Listed FDA GUDID 06959006302226
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cathay
- Generic name
- Transcutaneous electrical stimulation electrode, single-use
- Model / reference
- CM5050FB
- Primary DI / UDI-DI
- 06959006302226
- 510(k) Number
- FDA product code
- GXY
- GMDN term
- Transcutaneous electrical stimulation electrode, single-use
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
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