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FDA 510(k)

3TP WORKSPACE

K-Number: K050862 · 2005-07-25

Applicant3tp, LLC
Decision Date2005-07-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3TP WORKSPACE is the device name listed in this FDA 510(k) record. The listed applicant is 3tp, LLC. It received FDA 510(k) clearance on 2005-07-25 under 510(k) number K050862. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3TP WORKSPACE?

3TP WORKSPACE is a medical device that received FDA 510(k) clearance on 2005-07-25. The listed applicant is 3tp, LLC. The 510(k) number is K050862.

When did 3TP WORKSPACE receive FDA 510(k) clearance?

3TP WORKSPACE received FDA 510(k) clearance on 2005-07-25, under 510(k) number K050862.

Who is the listed applicant for 3TP WORKSPACE?

The FDA 510(k) record lists 3tp, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3TP WORKSPACE?

The FDA product code for 3TP WORKSPACE is LLZ.

Related Clinical Trials

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Other records listing 3tp, LLC 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.

K0313503TP SOFTWARE OPTION

Related Devices (Code: LLZ)

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.

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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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