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FDA 510(k)

LIAISON 25 TOTAL-D

K-Number: K132492 · 2013-09-05

ApplicantDiaSorin, Inc.
Decision Date2013-09-05
Product CodeMRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIAISON 25 TOTAL-D is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2013-09-05 under 510(k) number K132492. The device is classified under product code MRG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIAISON 25 TOTAL-D?

LIAISON 25 TOTAL-D is a medical device that received FDA 510(k) clearance on 2013-09-05. The listed applicant is DiaSorin, Inc.. The 510(k) number is K132492.

When did LIAISON 25 TOTAL-D receive FDA 510(k) clearance?

LIAISON 25 TOTAL-D received FDA 510(k) clearance on 2013-09-05, under 510(k) number K132492.

Who is the listed applicant for LIAISON 25 TOTAL-D?

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

What is the FDA product code for LIAISON 25 TOTAL-D?

The FDA product code for LIAISON 25 TOTAL-D is MRG.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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