FDA 510(k)

LIAISON XL ANALYZER MODEL 10050

K-Number: K103529 · 2011-01-21

Decision Date2011-01-21

Product CodeLOL

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

LIAISON XL ANALYZER MODEL 10050 is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2011-01-21 under 510(k) number K103529. The device is classified under product code LOL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIAISON XL ANALYZER MODEL 10050?

LIAISON XL ANALYZER MODEL 10050 is a medical device that received FDA 510(k) clearance on 2011-01-21. The listed applicant is DiaSorin, Inc.. The 510(k) number is K103529.

When did LIAISON XL ANALYZER MODEL 10050 receive FDA 510(k) clearance?

LIAISON XL ANALYZER MODEL 10050 received FDA 510(k) clearance on 2011-01-21, under 510(k) number K103529.

Who is the listed applicant for LIAISON XL ANALYZER MODEL 10050?

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 XL ANALYZER MODEL 10050?

The FDA product code for LIAISON XL ANALYZER MODEL 10050 is LOL.

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Other records listing DiaSorin, Inc. as applicant

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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.