StimelMD (SSMD) system
510(k) K260142
StimelMD (SSMD) system is a Class II device made by MOTION INFORMATICS Ltd., cleared under FDA 510(k) K260142 on 27 May 2026, 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 | NumberK260142 | Date27 May 2026 | StatusActive |
Official records
- FDA 510(k) database K260142
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IPF
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5850
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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