# DIA-H 1/2/3 & DIA-HT 1/2/3 (K840801)

_Diatech, Inc. · Apr 25, 1984 · HE · SESE_

**Canonical URL:** https://fda-staging.innolitics.com/device/K840801

## Device Facts

- **Applicant:** Diatech, Inc.
- **Decision Date:** Apr 25, 1984
- **Decision:** SESE
- **Submission Type:** Traditional
- **Review Panel:** HE

---

**Source:** [https://fda-staging.innolitics.com/device/K840801](https://fda-staging.innolitics.com/device/K840801)

**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