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FDA 510(k)

CHIROFLEX FORCEPS

K-Number: K903575 · 1990-12-21

ApplicantChiron Ophthalmics
Decision Date1990-12-21
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHIROFLEX FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Ophthalmics. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K903575. 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 CHIROFLEX FORCEPS?

CHIROFLEX FORCEPS is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Chiron Ophthalmics. The 510(k) number is K903575.

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

CHIROFLEX FORCEPS received FDA 510(k) clearance on 1990-12-21, under 510(k) number K903575.

Who is the listed applicant for CHIROFLEX FORCEPS?

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

What is the FDA product code for CHIROFLEX FORCEPS?

The FDA product code for CHIROFLEX FORCEPS is KYB.

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Other records listing Chiron Ophthalmics 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.

K915861MEDILENS-CS CORNEAL SHIELDK914311CHIROFLEX II LENS MICROSERT(TM)K905825COLLAGEN SHIELD, VARIOUS MODELSK903574CHIROFLEX LENS MICROSERTK901880MEDILENS(TM) CORNEAL SHIELDK894162OPTISOL

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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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