Solstice Xray Ring Marker Pad
510(k) K925892
Solstice Xray Ring Marker Pad is a Class I device made by Solstice Corp., cleared under FDA 510(k) K925892 on 18 May 1993, active as of 11 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 | NumberK925892 | Date18 May 1993 | StatusActive |
Official records
- FDA 510(k) database K925892
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAC
- Device class
- Class I
- Regulation
- 21 CFR Part 892.1640
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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