Blackrock Neuroport Biopotential Signal Processing System
by I2s Micro Implantable Systems, LLC 510(k)
Active
510(k) K090957
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK090957 | Date28 May 2009 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
-
- Terminated Z-2763-2016
- Terminated Z-2764-2016
Blackrock Microsystems, LLC announces a voluntary field action for the Blackrock NeuroPort Biopotential Signal Processing System because the Neural Signal Amplifier and the Patient Cable are incorrectly labeled as Type CF Applied Parts.
Specification
- 510(k) Number
- FDA Product Code
- GWL
- Device Class
- Class II
- Regulation
- 21 CFR Part 882.1835
- Advisory Committee
- Neurology
- FDA Decision
- SESE Substantially Equivalent