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FDA 510(k)

TENET RADIOLUCENT HAND TABLE

K-Number: K963506 · 1997-01-09

Decision Date1997-01-09
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TENET RADIOLUCENT HAND TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Tenet Medical Engineering. It received FDA 510(k) clearance on 1997-01-09 under 510(k) number K963506. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENET RADIOLUCENT HAND TABLE?

TENET RADIOLUCENT HAND TABLE is a medical device that received FDA 510(k) clearance on 1997-01-09. The listed applicant is Tenet Medical Engineering. The 510(k) number is K963506.

When did TENET RADIOLUCENT HAND TABLE receive FDA 510(k) clearance?

TENET RADIOLUCENT HAND TABLE received FDA 510(k) clearance on 1997-01-09, under 510(k) number K963506.

Who is the listed applicant for TENET RADIOLUCENT HAND TABLE?

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

What is the FDA product code for TENET RADIOLUCENT HAND TABLE?

The FDA product code for TENET RADIOLUCENT HAND TABLE is FQO.

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 Tenet Medical Engineering 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: FQO)

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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