Browse hierarchy: [Cardiovascular (CV)](/submissions/CV) → [Subpart B — Cardiovascular Diagnostic Devices](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices) → [21 CFR 870.1670](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/870.1670) → NKW — Actuator, Syringe, For Injector, Reprocessed

# NKW · Actuator, Syringe, For Injector, Reprocessed

_Cardiovascular · 21 CFR 870.1670 · Class 2_

**Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/NKW

## Overview

- **Product Code:** NKW
- **Device Name:** Actuator, Syringe, For Injector, Reprocessed
- **Regulation:** [21 CFR 870.1670](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/870.1670)
- **Device Class:** 2
- **Review Panel:** [Cardiovascular](/submissions/CV)
- **3rd-party reviewable:** yes

## Identification

Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

## Recent Cleared Devices (0 of 0)

_No cleared devices on record._

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**Source:** [https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/NKW](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/NKW)

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