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FDA 510(k)

ULTRA-VU ANGIOSCOPE

K-Number: K902329 · 1990-08-22

ApplicantAngiolaz, Inc.
Decision Date1990-08-22
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTRA-VU ANGIOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Angiolaz, Inc.. It received FDA 510(k) clearance on 1990-08-22 under 510(k) number K902329. 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 ULTRA-VU ANGIOSCOPE?

ULTRA-VU ANGIOSCOPE is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Angiolaz, Inc.. The 510(k) number is K902329.

When did ULTRA-VU ANGIOSCOPE receive FDA 510(k) clearance?

ULTRA-VU ANGIOSCOPE received FDA 510(k) clearance on 1990-08-22, under 510(k) number K902329.

Who is the listed applicant for ULTRA-VU ANGIOSCOPE?

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

What is the FDA product code for ULTRA-VU ANGIOSCOPE?

The FDA product code for ULTRA-VU ANGIOSCOPE is LYK.

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Other records listing Angiolaz, 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.

K994362HEADLAMP HL2000.K99244750 W METAL HALIDE ILLUMINATOR, VES 0501.K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEMK982409VES 1501-MK981819ANGIOLAZ VES-1CAMK981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR

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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.

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