Eview PV210
by Zhuhai Pusen Medical Technology Co, Ltd
Eview PV210 is a Class II device made by Zhuhai Pusen Medical Technology Co, Ltd, cleared under FDA 510(k) K190648 on 29 Mar 2019 and listed in FDA GUDID since 9 Apr 2019 (UDI-DI 06971176280043), 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 | Number06971176280043 | Date9 Apr 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK190648 | Date29 Mar 2019 | StatusActive |
Official records
- AccessGUDID record 06971176280043
- FDA 510(k) database K190648
Across registries
- FDA 510(k) K190648 decided 29 Mar 2019 Active
- FDA GUDID UDI-DI 06971176280043 listed 9 Apr 2019 Listed
Timeline
- Cleared FDA 510(k) K190648
- Listed FDA GUDID 06971176280043
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Eview
- Generic name
- Endoscopic video image processing unit
- Model / reference
- PV210
- Primary DI / UDI-DI
- 06971176280043
- 510(k) Number
- FDA product code
- FET
- GMDN term
- Endoscopic video image processing unit
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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