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FDA 510(k)

HIGH RISK

K-Number: K903559 · 1990-12-21

Decision Date1990-12-21
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HIGH RISK is the device name listed in this FDA 510(k) record. The listed applicant is Medical Resources, Ltd.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K903559. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH RISK?

HIGH RISK is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Medical Resources, Ltd.. The 510(k) number is K903559.

When did HIGH RISK receive FDA 510(k) clearance?

HIGH RISK received FDA 510(k) clearance on 1990-12-21, under 510(k) number K903559.

Who is the listed applicant for HIGH RISK?

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

What is the FDA product code for HIGH RISK?

The FDA product code for HIGH RISK is LYY.

Other records listing Medical Resources, 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.

View all 7 devices →

Related Devices (Code: LYY)

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.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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