← Product Code [BYI](/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYI) · K802646

# HAND PERCUSSOR CUP #65210 (K802646)

_B & F Medical Products, Inc. · BYI · Nov 12, 1980 · Anesthesiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYI/K802646

## Device Facts

- **Applicant:** B & F Medical Products, Inc.
- **Product Code:** [BYI](/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYI.md)
- **Decision Date:** Nov 12, 1980
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 868.5665
- **Device Class:** Class 2
- **Review Panel:** Anesthesiology

## Regulatory Identification

A powered percussor is a device that is intended to transmit vibration through a patient's chest wall to aid in freeing mucus deposits in the lung in order to improve bronchial drainage and that may be powered by electricity or compressed gas.

---

**Source:** [https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYI/K802646](https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYI/K802646)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
