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FDA 510(k)

IOL FORCEPS

K-Number: K821381 · 1982-06-14

ApplicantCilco, Inc.
Decision Date1982-06-14
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

IOL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K821381. 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 IOL FORCEPS?

IOL FORCEPS is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is Cilco, Inc.. The 510(k) number is K821381.

When did IOL FORCEPS receive FDA 510(k) clearance?

IOL FORCEPS received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821381.

Who is the listed applicant for IOL FORCEPS?

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

What is the FDA product code for IOL FORCEPS?

The FDA product code for IOL FORCEPS is KYB.

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Other records listing Cilco, Inc. as applicant

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.

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGEK854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K844249K-SOLK843319CILCO I/A SURGICAL PACKK843992CILCOR OPHTHALMIC INSTRUMENTSK843447CILCO DIAMOND KNIFE

View all 12 devices →

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.

K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786Duckworth & Kent, Ltd.K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2Duckworth & Kent, Ltd.K070669IOL INJECTOR SETMedicel AGK063155MONARCH III IOL DELIVERY SYSTEMAlcon Manufacturing, Ltd.K063694AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28Bausch & Lomb, Inc.K032412RE-USEABLE MICROSTAAR INJECTOR, MSI-SStaar Surgical Co.

Official Source

View on FDA Database →

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

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