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FDA 510(k)

BAILEY LENS SHOOTER

K-Number: K841730 · 1984-11-19

ApplicantIntermedics Intraocular, Inc.
Decision Date1984-11-19
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BAILEY LENS SHOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Intraocular, Inc.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K841730. 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 BAILEY LENS SHOOTER?

BAILEY LENS SHOOTER is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Intermedics Intraocular, Inc.. The 510(k) number is K841730.

When did BAILEY LENS SHOOTER receive FDA 510(k) clearance?

BAILEY LENS SHOOTER received FDA 510(k) clearance on 1984-11-19, under 510(k) number K841730.

Who is the listed applicant for BAILEY LENS SHOOTER?

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

What is the FDA product code for BAILEY LENS SHOOTER?

The FDA product code for BAILEY LENS SHOOTER is KYB.

Related Clinical Trials

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Other records listing Intermedics Intraocular, 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.

K862070INTER-SHARPK834543OCUCARE ULTRASOUND TIP & FREEDOM PACKK832525IRRIGATION/ASPIRATION PACK

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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