Medcaptain Life Science Co., Ltd.
Medcaptain Life Science Co., Ltd. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Dec 1, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 5 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 13, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K230528 | Extension Set | Dec 1, 2023 |
| K213004 | Needle Free Connector | May 10, 2022 |
| K202578 | KardiFlex NC Coronary Dilatation Catheter | May 6, 2021 |
| K202619 | KardiFlex PTCA Balloon Dilatation Catheter | Apr 29, 2021 |
| K202748 | Enteral Feeding Catheter | Apr 9, 2021 |
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