Mucheck V8
by Oncology Data Systems, Inc.
510(k) K091602
Mucheck V8 is a medical device (FDA Class II; FDA product code IYE, Accelerator, Linear, Medical) made by Oncology Data Systems, Inc., cleared under FDA 510(k) K091602 on 18 Jun 2009, 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 | NumberK091602 | Date18 Jun 2009 | StatusActive |
Official records
- FDA 510(k) database K091602
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IYE
- Device class
- Class II
- Regulation
- 21 CFR Part 892.5050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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