AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER— 510(k) K964406
Substantially EquivalentDaxor Corporation
FDA 510(k) clearance K964406 for AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER, Substantially Equivalent on 1997-09-25. Applicant: Daxor Corporation. Device class: 2.
Clearance details
- Applicant
- Daxor Corporation
- Product code
- Code JWO
- Device class
- Class 2
- Regulation
- 21 CFR 864.5950
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
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