N-Terminal HPTH by Ria

FDA 510(k) K811418 · Immuno Nuclear Corp.

Substantially Equivalent

510(k) numberK811418

Submission

Device name
N-Terminal HPTH by Ria
Applicant
Immuno Nuclear Corp.
Mchenry, IL, US
Received
May 19, 1981
Decision date
June 24, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K161158IDS-iSYS Intact PTHNCEW · Traditional Immunodiagnostic Systems , Ltd.01/31/2017SE
K150879LIASON 1-84 PTH Assay, LIASON 1-84 PTH Control Set, LIASON 1-84 PTH Calibration VerifiersCEW · Traditional DiaSorin, Inc.06/22/2015SE
K133601Advia Centaur Intact Parathyroid Hormone (Ipth) AssayCEW · Traditional Siemens Healthcare Diagnostics, Inc.02/05/2014SE
K132515Liaison N-Tact PTH Gen II, Control Set, Calibration VerifiersCEW · Traditional DiaSorin, Inc.11/08/2013SE
K121981Advia Centaur Inact Parathyroid Hormone (Ipth) AssayCEW · Traditional Siemens Healthcare Diagnostics03/21/2013SE

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Questions and answers

When was N-Terminal HPTH by Ria cleared by the FDA?

N-Terminal HPTH by Ria (K811418) received a 510(k) decision of Substantially Equivalent on June 24, 1981, 36 days after the submission was received.

What is the product code of K811418?

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