TEG 6s Hemostasis System, TEG 6s Citrated: K, RT, FF Assay Cartridge

FDA 510(k) K183160 · Haemonetics Corporation

Substantially Equivalent

510(k) numberK183160

Submission

Device name
TEG 6s Hemostasis System, TEG 6s Citrated: K, RT, FF Assay Cartridge
Applicant
Haemonetics Corporation
Braintree, MA, US
Received
November 15, 2018
Decision date
May 9, 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
JPA – System, Multipurpose For In Vitro Coagulation Studies
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5425
Specialty
Hematology

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More from Accriva Diagnostics, Inc.

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K251024TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay CartridgeJPA · Special 04/30/2025SE
K243858TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay CartridgeJPA · Special 01/15/2025SE
K232018Citrated: K, KH, RTH, FFHJPA · Traditional 03/29/2024SE
K221722Haemonetics Cell Saver Elite/Elite+ Autotransfusion System (CSE-E-US/CSE-EW-US)CAC · Traditional 11/15/2022SE
K160502TEG 6s Hemostasis SystemJPA · Special 04/19/2017SE
K162423Haemonetics Cell Saver Elite/Elite+ Autotransfusion SystemCAC · Traditional 01/03/2017SE
K160197Haemonetics Cell Saver Elite Autotransfusion SystemCAC · Traditional 05/24/2016SE
K122262Orthopat Advance Perioperative Autotransfusion SystemCAC · Traditional 10/25/2012SE
K120586Cell Saver EliteCAC · Traditional 05/22/2012SE
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Questions and answers

When was TEG 6s Hemostasis System, TEG 6s Citrated: K, RT, FF Assay Cartridge cleared by the FDA?

TEG 6s Hemostasis System, TEG 6s Citrated: K, RT, FF Assay Cartridge (K183160) received a 510(k) decision of Substantially Equivalent on May 9, 2019, 175 days after the submission was received.

What is the product code of K183160?

The FDA product code is JPA – System, Multipurpose For In Vitro Coagulation Studies, a Class II (moderate risk) device regulated under 21 CFR 864.5425.