← Product Code LFL · K851203

# R PAK (K851203)

_CooperVision, Inc. · LFL · Jul 23, 1985 · SU · SESE_

**Canonical URL:** https://fda.innolitics.com/device/K851203

## Device Facts

- **Applicant:** CooperVision, Inc.
- **Product Code:** LFL
- **Decision Date:** Jul 23, 1985
- **Decision:** SESE
- **Submission Type:** Traditional
- **Device Class:** Class U
- **Review Panel:** SU

---

**Source:** [https://fda.innolitics.com/device/K851203](https://fda.innolitics.com/device/K851203)

**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