DGB
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Seminal Fluid, Antigen, Antiserum, Control
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.5800
- Medical specialty
- Immunology
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| Record | Firm | Date | Builder |
|---|---|---|---|
| ZYGOTEK MICROCOMPUTERIZED SEMEN ANALYSIS SYSTEM (K861773) | Zygotek Systems, Inc. | 1986-07-07 | + Add |
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Every clearance here is in the API, with alerts when new ones post.