LANCER HDL SEPARATION KIT— 510(k) K790865
Substantially EquivalentSherwood Medical Co.
FDA 510(k) clearance K790865 for LANCER HDL SEPARATION KIT, Substantially Equivalent on 1979-06-28. Applicant: Sherwood Medical Co.. Device class: 1.
Clearance details
- Applicant
- Sherwood Medical Co.
- 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
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.