# Catheter, Thrombus Retriever
> **Product code: NRY** · Class II — Moderate Risk (510(k) clearance required) · Cardiovascular · 21 CFR 870.1250
## Classification
- **FDA Product Code:** NRY
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 870.1250
- **Review panel:** NE
- **Medical specialty:** Cardiovascular
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

The device is intended to restore blood flow by removing thrombus/clots in patients experiencing ischemic stroke.  The prior clearances in this category have been limited to simply identifying catheter placed in the peripheral, coronary, and neurovasculature.  It is felt that this is a unique claim and should not be combined with previously cleared catheters under a general procode.

## Market data
- **Cleared 510(k) submissions:** 106
- **Registered establishments:** 58
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=NRY)
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