LEECO GLYCO-HEMOGLOBIN DIAGNOSTIC KIT
FDA 510(k) clearance K791103 · decided 1979-06-28
Clearance details
- K-number
- K791103
- Device name
- LEECO GLYCO-HEMOGLOBIN DIAGNOSTIC KIT
- Applicant
- Leeco Diagnostics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-06-13
- Decision date
- 1979-06-28
- Days to decision
- 15 days
- Clearance type
- Traditional
- Product code
- LCP
- Device class
- 2
- Regulation number
- 864.7470
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.