# SGP Version 7.0 (Plasma Management System) (BK090082)

_Biomat USA, Inc. · Oct 1, 2010 · SESE_

**Canonical URL:** https://fda-staging.innolitics.com/device/BK090082

## Device Facts

- **Applicant:** Biomat USA, Inc.
- **Decision Date:** Oct 1, 2010
- **Decision:** SESE

---

**Source:** [https://fda-staging.innolitics.com/device/BK090082](https://fda-staging.innolitics.com/device/BK090082)

**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