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FDA 510(k)

THE ENDO OPTIKS MICROPROBE

K-Number: K924090 · 1993-02-01

ApplicantEndo Optics, Inc.
Decision Date1993-02-01
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE ENDO OPTIKS MICROPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Endo Optics, Inc.. It received FDA 510(k) clearance on 1993-02-01 under 510(k) number K924090. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ENDO OPTIKS MICROPROBE?

THE ENDO OPTIKS MICROPROBE is a medical device that received FDA 510(k) clearance on 1993-02-01. The listed applicant is Endo Optics, Inc.. The 510(k) number is K924090.

When did THE ENDO OPTIKS MICROPROBE receive FDA 510(k) clearance?

THE ENDO OPTIKS MICROPROBE received FDA 510(k) clearance on 1993-02-01, under 510(k) number K924090.

Who is the listed applicant for THE ENDO OPTIKS MICROPROBE?

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

What is the FDA product code for THE ENDO OPTIKS MICROPROBE?

The FDA product code for THE ENDO OPTIKS MICROPROBE is HQB.

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.

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Other records listing Endo Optics, 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.

K923600ENDO OPTIKS VALUE PACK

Related Devices (Code: HQB)

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.

K220263Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical ChandeliersVortex Surgical, Inc.K191846MAXReach Laser ProbeVortex Surgical, Inc.K182646Vitreq disposable laser probes, light fibers and ChandelierVitreQ BVK132614PEREGRINE CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K12299723GA CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K122905PEREGRINE 23GA CURVED LASER PROBEPeregrine Surgical , Ltd.

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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