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FDA 510(k)

3TP SOFTWARE OPTION

K-Number: K031350 · 2003-06-23

Applicant3tp, LLC
Decision Date2003-06-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3TP SOFTWARE OPTION is the device name listed in this FDA 510(k) record. The listed applicant is 3tp, LLC. It received FDA 510(k) clearance on 2003-06-23 under 510(k) number K031350. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3TP SOFTWARE OPTION?

3TP SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 2003-06-23. The listed applicant is 3tp, LLC. The 510(k) number is K031350.

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

3TP SOFTWARE OPTION received FDA 510(k) clearance on 2003-06-23, under 510(k) number K031350.

Who is the listed applicant for 3TP SOFTWARE OPTION?

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 SOFTWARE OPTION?

The FDA product code for 3TP SOFTWARE OPTION is LNH.

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.

K0508623TP WORKSPACE

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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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