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FDA 510(k)

ANGIOVISION VIEWING STATION

K-Number: K953972 · 1995-11-17

ApplicantMedivision Medical Imaging, Ltd.
Decision Date1995-11-17
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANGIOVISION VIEWING STATION is the device name listed in this FDA 510(k) record. The listed applicant is Medivision Medical Imaging, Ltd.. It received FDA 510(k) clearance on 1995-11-17 under 510(k) number K953972. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOVISION VIEWING STATION?

ANGIOVISION VIEWING STATION is a medical device that received FDA 510(k) clearance on 1995-11-17. The listed applicant is Medivision Medical Imaging, Ltd.. The 510(k) number is K953972.

When did ANGIOVISION VIEWING STATION receive FDA 510(k) clearance?

ANGIOVISION VIEWING STATION received FDA 510(k) clearance on 1995-11-17, under 510(k) number K953972.

Who is the listed applicant for ANGIOVISION VIEWING STATION?

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

What is the FDA product code for ANGIOVISION VIEWING STATION?

The FDA product code for ANGIOVISION VIEWING STATION is HKI.

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 Medivision Medical Imaging, Ltd. 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.

K062295IRI INTEGRATED RETINAL IMAGERK953974CAMVISION 1000K953973ANGIOVISION 1000

Related Devices (Code: HKI)

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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