CARDIOLIPIN G EIA TEST SYSTEM— 510(k) K946215
Substantially EquivalentHogan & Hartson
FDA 510(k) clearance K946215 for CARDIOLIPIN G EIA TEST SYSTEM, Substantially Equivalent on 1996-01-24. Applicant: Hogan & Hartson.
Clearance details
- Applicant
- Hogan & Hartson
- Product code
- Code MID
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, D.C., DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.