Ris Scanview System (Rsvs)
by Radiology Information Systems, Inc.
510(k) K970641
Ris Scanview System (Rsvs) is a medical device (FDA Class I; FDA product code LMD, System, Digital Image Communications, Radiological) made by Radiology Information Systems, Inc., cleared under FDA 510(k) K970641 on 2 May 1997, 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 | NumberK970641 | Date2 May 1997 | StatusActive |
Official records
- FDA 510(k) database K970641
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LMD
- Device class
- Class I
- Regulation
- 21 CFR Part 892.2020
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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