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FDA 510(k)

DESKS

K-Number: K926026 · 1993-03-24

Decision Date1993-03-24
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DESKS is the device name listed in this FDA 510(k) record. The listed applicant is Theradapt Products, Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K926026. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESKS?

DESKS is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Theradapt Products, Inc.. The 510(k) number is K926026.

When did DESKS receive FDA 510(k) clearance?

DESKS received FDA 510(k) clearance on 1993-03-24, under 510(k) number K926026.

Who is the listed applicant for DESKS?

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

What is the FDA product code for DESKS?

The FDA product code for DESKS is INW.

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 Theradapt 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.

Related Devices (Code: INW)

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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