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FDA 510(k)

FULL VIEW OMEGA TABLE

K-Number: K905827 · 1991-01-28

Decision Date1991-01-28
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FULL VIEW OMEGA TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tron Products, Inc.. It received FDA 510(k) clearance on 1991-01-28 under 510(k) number K905827. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FULL VIEW OMEGA TABLE?

FULL VIEW OMEGA TABLE is a medical device that received FDA 510(k) clearance on 1991-01-28. The listed applicant is Med-Tron Products, Inc.. The 510(k) number is K905827.

When did FULL VIEW OMEGA TABLE receive FDA 510(k) clearance?

FULL VIEW OMEGA TABLE received FDA 510(k) clearance on 1991-01-28, under 510(k) number K905827.

Who is the listed applicant for FULL VIEW OMEGA TABLE?

The FDA 510(k) record lists Med-Tron Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FULL VIEW OMEGA TABLE?

The FDA product code for FULL VIEW OMEGA TABLE is IYX.

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 Med-Tron Products, 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.

View all 9 devices →

Related Devices (Code: IYX)

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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