HEMATOLOGY COMPUTER-INTERFACE, VISCOUNT
FDA 510(k) clearance K822823 · decided 1982-10-18
Clearance details
- K-number
- K822823
- Device name
- HEMATOLOGY COMPUTER-INTERFACE, VISCOUNT
- Applicant
- Eko Scann AB
- Decision
- Substantially Equivalent
- Date received
- 1982-09-21
- Decision date
- 1982-10-18
- Days to decision
- 27 days
- Clearance type
- Traditional
- Product code
- LKM
- Device class
- 2
- Regulation number
- 864.5200
- 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.