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FDA 510(k)

MEDALIST EXAMINATION TABLE

K-Number: K883680 · 1988-10-04

Decision Date1988-10-04
Product CodeLGX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDALIST EXAMINATION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Industries, Inc.. It received FDA 510(k) clearance on 1988-10-04 under 510(k) number K883680. The device is classified under product code LGX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDALIST EXAMINATION TABLE?

MEDALIST EXAMINATION TABLE is a medical device that received FDA 510(k) clearance on 1988-10-04. The listed applicant is Hamilton Industries, Inc.. The 510(k) number is K883680.

When did MEDALIST EXAMINATION TABLE receive FDA 510(k) clearance?

MEDALIST EXAMINATION TABLE received FDA 510(k) clearance on 1988-10-04, under 510(k) number K883680.

Who is the listed applicant for MEDALIST EXAMINATION TABLE?

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

What is the FDA product code for MEDALIST EXAMINATION TABLE?

The FDA product code for MEDALIST EXAMINATION TABLE is LGX.

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.

Other records listing Hamilton Industries, 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.

Related Devices (Code: LGX)

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

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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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