Thrombelastograph (Teg) Platelet Mapping Assay

FDA 510(k) K041502 · Haemoscope Corp.

Substantially Equivalent

510(k) numberK041502

Submission

Device name
Thrombelastograph (Teg) Platelet Mapping Assay
Applicant
Haemoscope Corp.
Niles, IL, US
Received
June 7, 2004
Decision date
September 1, 2004
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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More from Chrono-Log Corp.

510(k)DeviceDecision
K062604Rapidteg Teg-Act TestJBP · Traditional 01/31/2007SE
K002177Thrombelastograph Coagulation Analyzer TEG-5000 SeriesJPA · Traditional 09/14/2000SE
K993678Thrombelastograph Coagulation Analyzer Teg - 5000 SeriesJPA · Traditional 05/05/2000SE
K954437Thrombelastograph Coagulation Analyzer 3000SGKP · Traditional 01/30/1996SE
K904204ThrombelastographGKP · Traditional 11/01/1990SE
K895844Thrombelastograph(R)GKP · Traditional 10/24/1989SE

Questions and answers

When was Thrombelastograph (Teg) Platelet Mapping Assay cleared by the FDA?

Thrombelastograph (Teg) Platelet Mapping Assay (K041502) received a 510(k) decision of Substantially Equivalent on September 1, 2004, 86 days after the submission was received.

What is the product code of K041502?

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