ALPCO Calprotectin Chemiluminescence ELISA, ALPCO Easy Stool Extraction Device

FDA 510(k) K191807 · Alpco

Substantially Equivalent

510(k) numberK191807

Submission

Device name
ALPCO Calprotectin Chemiluminescence ELISA, ALPCO Easy Stool Extraction Device
Applicant
Alpco
Salem, NH, US
Received
July 5, 2019
Decision date
October 25, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NXO – Calprotectin, Fecal
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5180
Specialty
Immunology

The device is used for the measurement, in human stool, of fecal calprotectin, a neutrophilic protein that is a marker of mucosal inflammation. The device can be used as an aid in the diagnosis of inflammatory bowel disease (ibd), crohn's disease and ulcerative colitis and to differentiate ibd from irritable bowel syndrome.

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Questions and answers

When was ALPCO Calprotectin Chemiluminescence ELISA, ALPCO Easy Stool Extraction Device cleared by the FDA?

ALPCO Calprotectin Chemiluminescence ELISA, ALPCO Easy Stool Extraction Device (K191807) received a 510(k) decision of Substantially Equivalent on October 25, 2019, 112 days after the submission was received.

What is the product code of K191807?

The FDA product code is NXO – Calprotectin, Fecal, a Class II (moderate risk) device regulated under 21 CFR 866.5180.