Varian/Ximatron 5 Carbon-Fiber Couch Top
510(k) K851653
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK851653 | Date23 May 1985 | StatusActive |
Recalls
-
- Terminated Z-0213-2008
Unexpected loss of Treatement Field Add-Ons (Wedges, Blocks, etc) during Ximatron simulation. If an unapproved treatment field is created without an MLC, but with an add-on, the add on will be deleted without warning. If this is not detected and corrected, incorrect dose delivery will occur.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- KPQ
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.5840
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent