Cleared Traditional

Lumpipulse G CA19-9-N

K191973 · Fujirebio Dianostics, Inc. · Immunology

Oct 2019

Decision

90d

Days

Class 2

Risk

About This 510(k) Submission

K191973 is an FDA 510(k) clearance for the Lumpipulse G CA19-9-N, a System, Test, Carbohydrate Antigen (ca19-9), For Monitoring And Management Of Pancreatic Cancer (Class II — Special Controls, product code NIG), submitted by Fujirebio Dianostics, Inc. (Malvern, US). The FDA issued a Cleared decision on October 22, 2019, 90 days after receiving the submission on July 24, 2019. This device falls under the Immunology review panel. Regulated under 21 CFR 866.6010.

Submission Details

510(k) Number	K191973 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 24, 2019
Decision Date	October 22, 2019
Days to Decision	90 days
Submission Type	Traditional
Review Panel	Immunology (IM)
Summary	Summary PDF

Device Classification

Product Code	NIG — System, Test, Carbohydrate Antigen (ca19-9), For Monitoring And Management Of Pancreatic Cancer
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 866.6010
Definition	An In Vitro Diagnostic Test For The Quantitative Measurement Of The Ca 19-9 Tumor Associated Antigen In Human Serum Or Plasma. The Test Is Intended As An Aid In The Management Of Patients With Confirmed Pancreatic Cancer And Serial Monitoring Of Their Response To Therapy And Disease Progression. The Test Should Only Be Used In Patients With Serum And Plasma Ca 19-9 Values Above The Cut-off At The Time Of Diagnosis And In Conjunction With Other Clinical Methods.