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FDA 510(k)

MCT COMPOSITE CHAIR

K-Number: K900191 · 1990-03-14

Decision Date1990-03-14
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MCT COMPOSITE CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Composite Technology, Inc.. It received FDA 510(k) clearance on 1990-03-14 under 510(k) number K900191. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCT COMPOSITE CHAIR?

MCT COMPOSITE CHAIR is a medical device that received FDA 510(k) clearance on 1990-03-14. The listed applicant is Medical Composite Technology, Inc.. The 510(k) number is K900191.

When did MCT COMPOSITE CHAIR receive FDA 510(k) clearance?

MCT COMPOSITE CHAIR received FDA 510(k) clearance on 1990-03-14, under 510(k) number K900191.

Who is the listed applicant for MCT COMPOSITE CHAIR?

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

What is the FDA product code for MCT COMPOSITE CHAIR?

The FDA product code for MCT COMPOSITE CHAIR is IOR.

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 Medical Composite Technology, 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: IOR)

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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