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FDA 510(k)

SHARP VIEW IMAGE ENHANCEMENT SYSTEM

K-Number: K024028 · 2003-01-24

ApplicantContext Vision AB
Decision Date2003-01-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHARP VIEW IMAGE ENHANCEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Context Vision AB. It received FDA 510(k) clearance on 2003-01-24 under 510(k) number K024028. 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 SHARP VIEW IMAGE ENHANCEMENT SYSTEM?

SHARP VIEW IMAGE ENHANCEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Context Vision AB. The 510(k) number is K024028.

When did SHARP VIEW IMAGE ENHANCEMENT SYSTEM receive FDA 510(k) clearance?

SHARP VIEW IMAGE ENHANCEMENT SYSTEM received FDA 510(k) clearance on 2003-01-24, under 510(k) number K024028.

Who is the listed applicant for SHARP VIEW IMAGE ENHANCEMENT SYSTEM?

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

What is the FDA product code for SHARP VIEW IMAGE ENHANCEMENT SYSTEM?

The FDA product code for SHARP VIEW IMAGE ENHANCEMENT SYSTEM 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 Context Vision AB 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.

K993802SHARPVIEW IMAGE ENHANCEMENT SYSTEM

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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