Interactive Real Time Scanning Package
by Siemens Medical Solutions USA, Inc.
510(k) K003623
Interactive Real Time Scanning Package is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K003623 on 21 Dec 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 | NumberK003623 | Date21 Dec 2000 | StatusActive |
Official records
- FDA 510(k) database K003623
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LNH
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1000
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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