Accu-Source
510(k) K051753
Accu-Source is a medical device (FDA Class II; FDA product code JAQ, System, Applicator, Radionuclide, Remote-Controlled) made by Oncology Systems, Inc., cleared under FDA 510(k) K051753 on 29 Mar 2006, 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 | NumberK051753 | Date29 Mar 2006 | StatusActive |
Official records
- FDA 510(k) database K051753
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAQ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.5700
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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