# ActiPatch

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/actipatch-pqy>
- Manufacturer: [Bioelectronics Corporation](https://devicerts.com/manufacturers/fda-fei-3005550216) (FDA registration: United States)
- Device class: Class II (US FDA)
- FDA product code: PQY

## Overview

*AI-generated summary, 2026-09-19. Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data is the record.*

ActiPatch is a nonthermal shortwave therapy device indicated for over-the-counter use for the treatment of pain. It is designed to provide pain relief for various conditions.

The device is supplied as a Class II medical device with FDA 510(k) clearance under product code PQY. It is intended for over-the-counter use and should be used according to the manufacturer's instructions.

## Registrations and authorizations

- **510(k)** · FDA 510(k) · United States · K192234 · decision 2020-01-31 · decision SESE · status: Active

## Recalls

No recall on record.

## Identifiers

- 510(k) Number: K192234 [FDA 510(k)]
- FDA product code: PQY [FDA 510(k)]

## Classification

- Device class: Class II [FDA 510(k)]
- Regulation: 21 CFR Part 890.5290 [FDA 510(k)]
- Advisory committee: Physical Medicine [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]

## Source and citation

- Cite as: ActiPatch, Bioelectronics Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/actipatch-pqy (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- Registry records last synced: 2026-10-06
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/actipatch-pqy.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/actipatch-pqy
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.