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FDA 510(k)

TIGRT MLC, TIGRT DMLC

K-Number: K090802 · 2009-07-07

ApplicantLinatech, LLC
Decision Date2009-07-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TIGRT MLC, TIGRT DMLC is the device name listed in this FDA 510(k) record. The listed applicant is Linatech, LLC. It received FDA 510(k) clearance on 2009-07-07 under 510(k) number K090802. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGRT MLC, TIGRT DMLC?

TIGRT MLC, TIGRT DMLC is a medical device that received FDA 510(k) clearance on 2009-07-07. The listed applicant is Linatech, LLC. The 510(k) number is K090802.

When did TIGRT MLC, TIGRT DMLC receive FDA 510(k) clearance?

TIGRT MLC, TIGRT DMLC received FDA 510(k) clearance on 2009-07-07, under 510(k) number K090802.

Who is the listed applicant for TIGRT MLC, TIGRT DMLC?

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

What is the FDA product code for TIGRT MLC, TIGRT DMLC?

The FDA product code for TIGRT MLC, TIGRT DMLC is IYE.

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.

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Other records listing Linatech, 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.

K232489VenusXK092550TIGRT IVSK090893TIGRT TPS

Related Devices (Code: IYE)

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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