Medscan 12
510(k) K933632
Medscan 12 is a Class II device made by Vidar Systems Corp., cleared under FDA 510(k) K933632 on 13 Dec 1993, active as of 10 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 | NumberK933632 | Date13 Dec 1993 | StatusActive |
Official records
- FDA 510(k) database K933632
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LMA
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2030
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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