MPP— 510(k) K131910
Substantially EquivalentMarc Pro
FDA 510(k) clearance K131910 for MPP, Substantially Equivalent on 2014-01-24. Applicant: Marc Pro. Device class: 2.
Clearance details
- Applicant
- Marc Pro
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.