Cathay GP202S-Ac
by Cathay Manufacturing Corp. 2 variants
Cathay GP202S-Ac is a Class II device made by Cathay Manufacturing Corp., cleared under FDA 510(k) K130027 on 22 Aug 2013 and listed in FDA GUDID since 29 Oct 2020 (UDI-DI 06959006303292), 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 | Number06959006303292 | Date29 Oct 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK130027 | Date22 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 06959006303292
- FDA 510(k) database K130027
Across registries
- FDA 510(k) K130027 decided 22 Aug 2013 Active
- FDA GUDID UDI-DI 06959006303292 listed 29 Oct 2020 Listed
Timeline
- Cleared FDA 510(k) K130027
- Listed FDA GUDID 06959006303292
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cathay
- Generic name
- Electrosurgical return electrode, single-use
- Model / reference
- GP202S-AC
- Primary DI / UDI-DI
- 06959006303292
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electrosurgical return electrode, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Electrosurgical return electrode, single-use.
- MACROLYTE 400-2100 by Conmed Corporation
- THERMOGARD 51-7410 by Conmed Corporation
- Tosap Plate 26189190 by Tolu Sadrneshinan Pars
- Olympus WA99516C by Olympus Winter & Ibe GmbH
- Olympus WA99514C by Olympus Winter & Ibe GmbH
- Bovie ESRE by Aspen Surgical Products, Inc.
- ERBE 20193-075 by Erbe Elektromedizin GmbH
- F7320W/V by FIAB S.p.A.
- RF-DGP-IS by ST. JUDE MEDICAL, INC.
- Disposable Patient Plate HPP221 by ZHEJIANG HAISHENG MEDICAL DEVICE CO., LTD.