← Product Code [BYP](/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYP) · K840459

# IMPROVED MOUTHPIECE (K840459)

_Kinetix · BYP · Feb 17, 1984 · Anesthesiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYP/K840459

## Device Facts

- **Applicant:** Kinetix
- **Product Code:** [BYP](/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYP.md)
- **Decision Date:** Feb 17, 1984
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 868.5620
- **Device Class:** Class 1
- **Review Panel:** Anesthesiology

## Regulatory Identification

A breathing mouthpiece is a rigid device that is inserted into a patient's mouth and that connects with diagnostic or therapeutic respiratory devices.

---

**Source:** [https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYP/K840459](https://fda.innolitics.com/submissions/AN/subpart-f%E2%80%94therapeutic-devices/BYP/K840459)

**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
