Platelet Aggregating Reagents

FDA 510(k) K780047 · Dade, Baxter Travenol Diagnostics, Inc.

Substantially Equivalent

510(k) numberK780047

Submission

Device name
Platelet Aggregating Reagents
Applicant
Dade, Baxter Travenol Diagnostics, Inc.
Mchenry, IL, US
Received
January 9, 1978
Decision date
March 2, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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

More from Chrono-Log Corp.

510(k)DeviceDecision
K800296Whole Blood Gas Control, Levels 1,2,&3GGM · Traditional 03/05/1980SE
K792606Whole Blood Platelet Control Normal,JPK · Traditional 02/13/1980SE
K792723Blood Fluid FiltersJKA · Traditional 01/21/1980SE
K792607T3 Uptake (T3U) ReagentsKHQ · Traditional 01/16/1980SE
K792443TSH RadioimmunoassayJLW · Traditional 12/27/1979SE
K792442Ferritin RadioimmunoassayDBF · Traditional 12/18/1979SE
K791922Harleco Brand Clinicard Lipase Test SetCET · Traditional 11/27/1979SE
K792183Dade High Density Lipoprotein CholesteroLBS · Traditional 11/13/1979SE
K790776Dade Low Ionic Strength Soluition (Liss)KSG · Traditional 05/23/1979SE
K790767Immu-Tek Automatic CentrifugeKSN · Traditional 05/23/1979SE

Questions and answers

When was Platelet Aggregating Reagents cleared by the FDA?

Platelet Aggregating Reagents (K780047) received a 510(k) decision of Substantially Equivalent on March 2, 1978, 52 days after the submission was received.

What is the product code of K780047?

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