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FDA 510(k)

IMAGE TRANSPORT SERIES II

K-Number: K925963 · 1995-02-03

ApplicantDataview Imaging Intl., Inc.
Decision Date1995-02-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGE TRANSPORT SERIES II is the device name listed in this FDA 510(k) record. The listed applicant is Dataview Imaging Intl., Inc.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K925963. 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 IMAGE TRANSPORT SERIES II?

IMAGE TRANSPORT SERIES II is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Dataview Imaging Intl., Inc.. The 510(k) number is K925963.

When did IMAGE TRANSPORT SERIES II receive FDA 510(k) clearance?

IMAGE TRANSPORT SERIES II received FDA 510(k) clearance on 1995-02-03, under 510(k) number K925963.

Who is the listed applicant for IMAGE TRANSPORT SERIES II?

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

What is the FDA product code for IMAGE TRANSPORT SERIES II?

The FDA product code for IMAGE TRANSPORT SERIES II is LLZ.

Related Clinical Trials

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Other records listing Dataview Imaging Intl., 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.

K925964IMAGE TRANSPORT SERIES III

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.

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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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