Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AMETEC MASY MODULAR ANGIOSCOPE SYSTEM

K-Number: K905745 · 1992-04-23

ApplicantAmerican Medical Technology, Inc.
Decision Date1992-04-23
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMETEC MASY MODULAR ANGIOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Technology, Inc.. It received FDA 510(k) clearance on 1992-04-23 under 510(k) number K905745. The device is classified under product code LYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMETEC MASY MODULAR ANGIOSCOPE SYSTEM?

AMETEC MASY MODULAR ANGIOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1992-04-23. The listed applicant is American Medical Technology, Inc.. The 510(k) number is K905745.

When did AMETEC MASY MODULAR ANGIOSCOPE SYSTEM receive FDA 510(k) clearance?

AMETEC MASY MODULAR ANGIOSCOPE SYSTEM received FDA 510(k) clearance on 1992-04-23, under 510(k) number K905745.

Who is the listed applicant for AMETEC MASY MODULAR ANGIOSCOPE SYSTEM?

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

What is the FDA product code for AMETEC MASY MODULAR ANGIOSCOPE SYSTEM?

The FDA product code for AMETEC MASY MODULAR ANGIOSCOPE SYSTEM is LYK.

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 American Medical Technology, 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.

K963808CHOICE POWERED WHEELCHAIRK874567RESUSCITATORK874430NEEDLE CONTAINERK874360PLASTIC TUBING CONNECTORK873313SURGICAL DRAPE

Related Devices (Code: LYK)

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.

K253842Vena MicroAngioscope™ SystemVena Medical Holdings CorpK251767Vena MicroAngioscope™ SystemVena Medical Holdings CorpK062340CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEMCardio-Optics, Inc.K050808CORONARY SINUS ACCESS KIT, MODEL KCS8F-01Cardio-Optics, Inc.K011793KSEA FIBERSCOPEKARL STORZ Endoscopy-America, Inc.K012724SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273Smith & Nephew, Inc.

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.

↑