LMQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Peritoneal Access, Subcutaneous, Implanted
- Device class
- Class III (high risk)
- Medical specialty
- Unknown
- Flags
- Implant
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| Record | Firm | Date | Builder |
|---|---|---|---|
| NORFOLK MEDICAL PERITONEAL-ACCESS PORT (K854593) | Norfolk Medical Products, Inc. | 1986-02-04 | + Add |
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Every clearance here is in the API, with alerts when new ones post.