# I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI (K853242)

_U.S. Mfg. & Management, Inc. · Aug 30, 1985 · SU · SESD_

**Canonical URL:** https://fda-staging.innolitics.com/device/K853242

## Device Facts

- **Applicant:** U.S. Mfg. & Management, Inc.
- **Decision Date:** Aug 30, 1985
- **Decision:** SESD
- **Submission Type:** Traditional
- **Review Panel:** SU

---

**Source:** [https://fda-staging.innolitics.com/device/K853242](https://fda-staging.innolitics.com/device/K853242)

**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