← Product Code [EXA](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EXA) · K781736

# DISC, COLOPLAST PRE-OP STOMA (K781736)

_C.R. Bard, Inc. · EXA · Nov 3, 1978 · Gastroenterology, Urology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EXA/K781736

## Device Facts

- **Applicant:** C.R. Bard, Inc.
- **Product Code:** [EXA](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EXA.md)
- **Decision Date:** Nov 3, 1978
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 876.5900
- **Device Class:** Class 1
- **Review Panel:** Gastroenterology, Urology

---

**Source:** [https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EXA/K781736](https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EXA/K781736)

**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