LEECO LH-QUANT DIAGNOSTIC KIT— 510(k) K810662
Substantially EquivalentLeeco Diagnostics, Inc.
FDA 510(k) clearance K810662 for LEECO LH-QUANT DIAGNOSTIC KIT, Substantially Equivalent on 1981-03-31. Applicant: Leeco Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- Leeco Diagnostics, Inc.
- Product code
- Code CEP
- Device class
- Class 1
- Regulation
- 21 CFR 862.1485
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code CEP
view allMore clearances from Leeco Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.