Proview Medical Image Display Module
by Cerner Corp.
510(k) K000770
Proview Medical Image Display Module is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Cerner Corp., cleared under FDA 510(k) K000770 on 16 May 2000, 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 | FDA 510(k)SESE | NumberK000770 | Date16 May 2000 | StatusActive |
Official records
- FDA 510(k) database K000770
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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