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FDA 510(k)

REAL-TIME VIDEO CONTRAST ENHANCER

K-Number: K962260 · 1996-09-09

ApplicantDigivision, Inc.
Decision Date1996-09-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REAL-TIME VIDEO CONTRAST ENHANCER is the device name listed in this FDA 510(k) record. The listed applicant is Digivision, Inc.. It received FDA 510(k) clearance on 1996-09-09 under 510(k) number K962260. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAL-TIME VIDEO CONTRAST ENHANCER?

REAL-TIME VIDEO CONTRAST ENHANCER is a medical device that received FDA 510(k) clearance on 1996-09-09. The listed applicant is Digivision, Inc.. The 510(k) number is K962260.

When did REAL-TIME VIDEO CONTRAST ENHANCER receive FDA 510(k) clearance?

REAL-TIME VIDEO CONTRAST ENHANCER received FDA 510(k) clearance on 1996-09-09, under 510(k) number K962260.

Who is the listed applicant for REAL-TIME VIDEO CONTRAST ENHANCER?

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

What is the FDA product code for REAL-TIME VIDEO CONTRAST ENHANCER?

The FDA product code for REAL-TIME VIDEO CONTRAST ENHANCER is LLZ.

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 Digivision, 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.

K895320FLUOROVISION HR 2000 HIGH RESOLUTION IMAGE ENHANCEK873646DIGIVIEWERK864584FLUOROVISION CONTRAST ENHANCER

Related Devices (Code: LLZ)

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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