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FDA 510(k)

MORGAN THERAPEUTIC LENS

K-Number: K871454 · 1987-06-19

ApplicantMortan, Inc.
Decision Date1987-06-19
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MORGAN THERAPEUTIC LENS is the device name listed in this FDA 510(k) record. The listed applicant is Mortan, Inc.. It received FDA 510(k) clearance on 1987-06-19 under 510(k) number K871454. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORGAN THERAPEUTIC LENS?

MORGAN THERAPEUTIC LENS is a medical device that received FDA 510(k) clearance on 1987-06-19. The listed applicant is Mortan, Inc.. The 510(k) number is K871454.

When did MORGAN THERAPEUTIC LENS receive FDA 510(k) clearance?

MORGAN THERAPEUTIC LENS received FDA 510(k) clearance on 1987-06-19, under 510(k) number K871454.

Who is the listed applicant for MORGAN THERAPEUTIC LENS?

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

What is the FDA product code for MORGAN THERAPEUTIC LENS?

The FDA product code for MORGAN THERAPEUTIC LENS is KYG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Mortan, 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.

K821897LENS

Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, Inc.

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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