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FDA 510(k)

SERIES V-SCAN RADIOGRAPHIC FILM SCANNER

K-Number: K925664 · 1993-06-22

ApplicantVision Ten, Inc.
Decision Date1993-06-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SERIES V-SCAN RADIOGRAPHIC FILM SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Vision Ten, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K925664. 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 SERIES V-SCAN RADIOGRAPHIC FILM SCANNER?

SERIES V-SCAN RADIOGRAPHIC FILM SCANNER is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Vision Ten, Inc.. The 510(k) number is K925664.

When did SERIES V-SCAN RADIOGRAPHIC FILM SCANNER receive FDA 510(k) clearance?

SERIES V-SCAN RADIOGRAPHIC FILM SCANNER received FDA 510(k) clearance on 1993-06-22, under 510(k) number K925664.

Who is the listed applicant for SERIES V-SCAN RADIOGRAPHIC FILM SCANNER?

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

What is the FDA product code for SERIES V-SCAN RADIOGRAPHIC FILM SCANNER?

The FDA product code for SERIES V-SCAN RADIOGRAPHIC FILM SCANNER 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 Vision Ten, 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.

K894412RADIOSCOPE OR MAMMOSCOPE

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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