Electro Interstitial Scan
510(k) K102166
Electro Interstitial Scan is a Class II device made by Ld Technology, LLC, cleared under FDA 510(k) K102166 on 10 Dec 2010, 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 | NumberK102166 | Date10 Dec 2010 | StatusActive |
Official records
- FDA 510(k) database K102166
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GZO
- Device class
- Class II
- Regulation
- 21 CFR Part 882.1540
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
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