IDS-iSYS Intact PTHN

FDA 510(k) K161158 · Immunodiagnostic Systems , Ltd.

Substantially Equivalent

510(k) numberK161158

Submission

Device name
IDS-iSYS Intact PTHN
Applicant
Immunodiagnostic Systems , Ltd.
Boldon, GB
Received
April 25, 2016
Decision date
January 31, 2017
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 IDS-iSYS Intact PTHN cleared by the FDA?

IDS-iSYS Intact PTHN (K161158) received a 510(k) decision of Substantially Equivalent on January 31, 2017, 281 days after the submission was received.

What is the product code of K161158?

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