AESKULISA GLIA A AND AESKULISA GLIA G— 510(k) K052439
Substantially EquivalentAesku Diagnostics
FDA 510(k) clearance K052439 for AESKULISA GLIA A AND AESKULISA GLIA G, Substantially Equivalent on 2006-02-07. Applicant: Aesku Diagnostics. Device class: 2.
Clearance details
- Applicant
- Aesku Diagnostics
- Product code
- Code MST
- Device class
- Class 2
- Regulation
- 21 CFR 866.5750
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
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More clearances from Aesku Diagnostics
view allData sourced from openFDA. This site is unofficial and independent of the FDA.