← Product Code [HQL](/submissions/OP/subpart-d%E2%80%94prosthetic-devices/HQL) · P890068

# MODEL P-11 MODIFIED J-LOOP POSTERIOR CHAMBER IOL (P890068)

_Chiron Ophthalmics · HQL · Jan 11, 1990 · Ophthalmic · APPR_

**Canonical URL:** https://fda.innolitics.com/submissions/OPHTHALMIC/subpart-d%E2%80%94prosthetic-devices/HQL/P890068

## Device Facts

- **Applicant:** Chiron Ophthalmics
- **Product Code:** [HQL](/submissions/OP/subpart-d%E2%80%94prosthetic-devices/HQL.md)
- **Decision Date:** Jan 11, 1990
- **Decision:** APPR
- **Regulation:** 21 CFR 886.3600
- **Device Class:** Class 3
- **Review Panel:** Ophthalmic

## Regulatory Identification

An intraocular lens is a device made of materials such as glass or plastic intended to be implanted to replace the natural lens of an eye.

---

**Source:** [https://fda.innolitics.com/submissions/OPHTHALMIC/subpart-d%E2%80%94prosthetic-devices/HQL/P890068](https://fda.innolitics.com/submissions/OPHTHALMIC/subpart-d%E2%80%94prosthetic-devices/HQL/P890068)

**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