Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE

K-Number: K903921 · 1990-12-04

Decision Date1990-12-04
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Imt America, Inc.. It received FDA 510(k) clearance on 1990-12-04 under 510(k) number K903921. The device is classified under product code IZZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE?

MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE is a medical device that received FDA 510(k) clearance on 1990-12-04. The listed applicant is Imt America, Inc.. The 510(k) number is K903921.

When did MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE receive FDA 510(k) clearance?

MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE received FDA 510(k) clearance on 1990-12-04, under 510(k) number K903921.

Who is the listed applicant for MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE?

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

What is the FDA product code for MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE?

The FDA product code for MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE is IZZ.

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 Imt America, 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: IZZ)

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.

↑