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FDA 510(k)

VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM

K-Number: K890047 · 1989-06-20

ApplicantVascucare, Inc.
Decision Date1989-06-20
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vascucare, Inc.. It received FDA 510(k) clearance on 1989-06-20 under 510(k) number K890047. 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 VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM?

VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-06-20. The listed applicant is Vascucare, Inc.. The 510(k) number is K890047.

When did VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM receive FDA 510(k) clearance?

VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM received FDA 510(k) clearance on 1989-06-20, under 510(k) number K890047.

Who is the listed applicant for VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM?

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

What is the FDA product code for VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM?

The FDA product code for VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY 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.

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Other records listing Vascucare, 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.

K883158RESPIRATORY AIRWAY TUBE MONITOR (RATM)K881780VASCUCARE ANGIOPUMP

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

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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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