Liaison N-Tact PTH

FDA 510(k) K033426 · DiaSorin, Inc.

Substantially Equivalent

510(k) numberK033426

Submission

Device name
Liaison N-Tact PTH
Applicant
DiaSorin, Inc.
Stillwater, MN, US
Received
October 27, 2003
Decision date
February 12, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CEW – Radioimmunoassay, Parathyroid Hormone
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1545
Specialty
Clinical Chemistry

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Questions and answers

When was Liaison N-Tact PTH cleared by the FDA?

Liaison N-Tact PTH (K033426) received a 510(k) decision of Substantially Equivalent on February 12, 2004, 108 days after the submission was received.

What is the product code of K033426?

The FDA product code is CEW – Radioimmunoassay, Parathyroid Hormone, a Class II (moderate risk) device regulated under 21 CFR 862.1545.