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FDA 510(k)

THE MIDVIEW-MEDCON'S DICOM VIEWER

K-Number: K971181 · 1997-07-29

ApplicantMedcon , Ltd.
Decision Date1997-07-29
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THE MIDVIEW-MEDCON'S DICOM VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Medcon , Ltd.. It received FDA 510(k) clearance on 1997-07-29 under 510(k) number K971181. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MIDVIEW-MEDCON'S DICOM VIEWER?

THE MIDVIEW-MEDCON'S DICOM VIEWER is a medical device that received FDA 510(k) clearance on 1997-07-29. The listed applicant is Medcon , Ltd.. The 510(k) number is K971181.

When did THE MIDVIEW-MEDCON'S DICOM VIEWER receive FDA 510(k) clearance?

THE MIDVIEW-MEDCON'S DICOM VIEWER received FDA 510(k) clearance on 1997-07-29, under 510(k) number K971181.

Who is the listed applicant for THE MIDVIEW-MEDCON'S DICOM VIEWER?

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

What is the FDA product code for THE MIDVIEW-MEDCON'S DICOM VIEWER?

The FDA product code for THE MIDVIEW-MEDCON'S DICOM VIEWER is IZI.

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Other records listing Medcon , Ltd. as applicant

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Related Devices (Code: IZI)

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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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