T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01

FDA 510(k) K191364 · Fujimori Kogyo, Co., Ltd.

Substantially Equivalent

510(k) numberK191364

Submission

Device name
T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01
Applicant
Fujimori Kogyo, Co., Ltd.
Shinjuku, Tokyo, JP
Received
May 22, 2019
Decision date
February 14, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOZ – System, Automated Platelet Aggregation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5700
Specialty
Hematology

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K161329Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channelJOZ · Special Chrono-Log Corp.12/02/2016SE
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K122162AggreguideJOZ · Traditional Aggredyne, Inc.12/20/2013SE
K103555Multiplate 5.0 AggregometerJOZ · Traditional Verum Diagnostica GmbH07/27/2012SE
K060489Dade PFA-100 Platelet Function Analyzer and ReagentsJOZ · Traditional Dade Behring, Inc.07/21/2006SE
K050265Chrono-Log Whole Blood Lumi-Aggregometer, Model 700JOZ · Traditional Chrono-Log Corp.10/14/2005SE
K051231VERIFYNOW-P2Y12 AssayJOZ · Traditional Accumetrics, Inc.08/05/2005SE

Questions and answers

When was T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01 cleared by the FDA?

T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01 (K191364) received a 510(k) decision of Substantially Equivalent on February 14, 2020, 268 days after the submission was received.

What is the product code of K191364?

The FDA product code is JOZ – System, Automated Platelet Aggregation, a Class II (moderate risk) device regulated under 21 CFR 864.5700.