INSPIRA HD, MODEL: NL1000— 510(k) K090811
Substantially EquivalentNeurologica Corporation
FDA 510(k) clearance K090811 for INSPIRA HD, MODEL: NL1000, Substantially Equivalent on 2009-08-27. Applicant: Neurologica Corporation. Device class: 2.
Clearance details
- Applicant
- Neurologica Corporation
- Product code
- Code KPS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1200
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Danvers, MA, US
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