Angioslide, Ltd.
Angioslide, Ltd. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Dec 15, 2017
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 6 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 23, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K172494 | PROTEUS PTA Balloon Catheter with Embolic Capture Feature | Dec 15, 2017 |
| K133043 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE | Dec 6, 2013 |
| K120164 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE | Jun 8, 2012 |
| K120805 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE | Apr 13, 2012 |
| K111750 | EXTRA PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE; PROTEUS PTA BALLOON CATHETER WITH EMBOLIC… | Jul 21, 2011 |
| K090364 | EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATURE | Mar 23, 2010 |