Product code KSO
- Device name
- Centrifuge, Blood-Bank For In Vitro Diagnostic Use
- Medical specialty
- Hematology
- Device class
- 1
- Regulation number
- 864.9275
- Review panel
- HE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K780281 | IMMUFUGE DISP. LINER | Dade, Baxter Travenol Diagnostics, Inc. | 1978-03-02 |
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