← Product Code [LXW](/productcode/LXW) · K895881

# MOTIONSPECT (K895881)

_Baltimore Therapeutic Equipment Co. · LXW · Apr 10, 1990 · GU · SESE_

**Canonical URL:** https://fda.innolitics.com/device/K895881

## Device Facts

- **Applicant:** Baltimore Therapeutic Equipment Co.
- **Product Code:** [LXW](/productcode/LXW.md)
- **Decision Date:** Apr 10, 1990
- **Decision:** SESE
- **Submission Type:** Traditional
- **Device Class:** Class 3
- **Review Panel:** GU

---

**Source:** [https://fda.innolitics.com/device/K895881](https://fda.innolitics.com/device/K895881)

**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
