← Product Code [MVF](/productcode/MVF) · P990021S001

# DIOMED 630 PDT LASER (P990021S001)

_Pinnacle Biologics, Inc. · MVF · Aug 1, 2003 · General, Plastic Surgery · APPR_

**Canonical URL:** https://fda-staging.innolitics.com/device/P990021S001

## Device Facts

- **Applicant:** Pinnacle Biologics, Inc.
- **Product Code:** [MVF](/productcode/MVF.md)
- **Decision Date:** Aug 1, 2003
- **Decision:** APPR
- **Device Class:** Class 3
- **Review Panel:** General, Plastic Surgery

---

**Source:** [https://fda-staging.innolitics.com/device/P990021S001](https://fda-staging.innolitics.com/device/P990021S001)

**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 PMA](https://innolitics.com/services/regulatory/), [a 510(k)](https://innolitics.com/services/510ks/), [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