Disposable Passive Array - Blunt Probe MP1000
Disposable Passive Array - Blunt Probe MP1000 is a Class II device made by Izi Medical Products LLC, cleared under FDA 510(k) K142344 on 20 Mar 2015 and listed in FDA GUDID since 4 Nov 2016 (UDI-DI 00815212020360), 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 | GUDID listing | Number00815212020360 | Date4 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142344 | Date20 Mar 2015 | StatusActive |
Official records
- AccessGUDID record 00815212020360
- FDA 510(k) database K142344
Across registries
- FDA 510(k) K142344 decided 20 Mar 2015 Active
- FDA GUDID UDI-DI 00815212020360 listed 4 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K142344
- Listed FDA GUDID 00815212020360
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Disposable Passive Array - Blunt Probe
- Generic name
- Neurological stereotactic surgery system
- Model / reference
- MP1000
- Primary DI / UDI-DI
- 00815212020360
- 510(k) Number
- FDA product code
- HAW
- GMDN term
- Neurological stereotactic surgery system
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
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