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FDA 510(k)

TRUST DAM

K-Number: K091769 · 2010-02-05

Decision Date2010-02-05
Product CodeMSC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TRUST DAM is the device name listed in this FDA 510(k) record. The listed applicant is Line One Laboratories, Inc.. It received FDA 510(k) clearance on 2010-02-05 under 510(k) number K091769. The device is classified under product code MSC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUST DAM?

TRUST DAM is a medical device that received FDA 510(k) clearance on 2010-02-05. The listed applicant is Line One Laboratories, Inc.. The 510(k) number is K091769.

When did TRUST DAM receive FDA 510(k) clearance?

TRUST DAM received FDA 510(k) clearance on 2010-02-05, under 510(k) number K091769.

Who is the listed applicant for TRUST DAM?

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

What is the FDA product code for TRUST DAM?

The FDA product code for TRUST DAM is MSC.

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.

Related Devices (Code: MSC)

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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