Gsd GP900A
by Shenzhen GSD Tech Co., Ltd.
Gsd GP900A is a Class II device made by Shenzhen GSD Tech Co., Ltd., cleared under FDA 510(k) K142186 on 17 Apr 2015 and listed in FDA GUDID since 30 Sep 2024 (UDI-DI 06928258000907), 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 | Number06928258000907 | Date30 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142186 | Date17 Apr 2015 | StatusActive |
Official records
- AccessGUDID record 06928258000907
- FDA 510(k) database K142186
Across registries
- FDA 510(k) K142186 decided 17 Apr 2015 Active
- FDA GUDID UDI-DI 06928258000907 listed 30 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K142186
- Listed FDA GUDID 06928258000907
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Gsd
- Generic name
- Dermatological diode laser system
- Model / reference
- GP900A
- Primary DI / UDI-DI
- 06928258000907
- 510(k) Number
- FDA product code
- GEX
- GMDN term
- Dermatological diode laser system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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