ICA PLASMA HDL AND LDL MEASUREMENT SYSTEM— 510(k) K903733
Substantially EquivalentInstitute For Clinical Applications
FDA 510(k) clearance K903733 for ICA PLASMA HDL AND LDL MEASUREMENT SYSTEM, Substantially Equivalent on 1991-01-15. Applicant: Institute For Clinical Applications. Device class: 1.
Clearance details
- Applicant
- Institute For Clinical Applications
- Product code
- Code LBR
- Device class
- Class 1
- Regulation
- 21 CFR 862.1475
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.