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FDA 510(k)

I-GLIDE IOL IMPLANTATION AID

K-Number: K832939 · 1983-10-04

ApplicantI For M, Inc.
Decision Date1983-10-04
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

I-GLIDE IOL IMPLANTATION AID is the device name listed in this FDA 510(k) record. The listed applicant is I For M, Inc.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832939. The device is classified under product code KYB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I-GLIDE IOL IMPLANTATION AID?

I-GLIDE IOL IMPLANTATION AID is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is I For M, Inc.. The 510(k) number is K832939.

When did I-GLIDE IOL IMPLANTATION AID receive FDA 510(k) clearance?

I-GLIDE IOL IMPLANTATION AID received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832939.

Who is the listed applicant for I-GLIDE IOL IMPLANTATION AID?

The FDA 510(k) record lists I For M, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I-GLIDE IOL IMPLANTATION AID?

The FDA product code for I-GLIDE IOL IMPLANTATION AID is KYB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: KYB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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