← Product Code [KYB](/submissions/OP/subpart-e%E2%80%94surgical-devices/KYB) · K832939

# I-GLIDE IOL IMPLANTATION AID (K832939)

_I For M, Inc. · KYB · Oct 4, 1983 · Ophthalmic · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/OP/subpart-e%E2%80%94surgical-devices/KYB/K832939

## Device Facts

- **Applicant:** I For M, Inc.
- **Product Code:** [KYB](/submissions/OP/subpart-e%E2%80%94surgical-devices/KYB.md)
- **Decision Date:** Oct 4, 1983
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 886.4300
- **Device Class:** Class 1
- **Review Panel:** Ophthalmic

## Regulatory Identification

An intraocular lens guide is a device intended to be inserted into the eye during surgery to direct the insertion of an intraocular lens and be removed after insertion is completed.

---

**Source:** [https://fda.innolitics.com/submissions/OP/subpart-e%E2%80%94surgical-devices/KYB/K832939](https://fda.innolitics.com/submissions/OP/subpart-e%E2%80%94surgical-devices/KYB/K832939)

**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
