Reagent, Firefly #395

FDA 510(k) K781807 · Chrono-Log Corp.

Substantially Equivalent

510(k) numberK781807

Submission

Device name
Reagent, Firefly #395
Applicant
Chrono-Log Corp.
Havertown, PA, US
Received
October 25, 1978
Decision date
November 22, 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

Other 510(k)s with product code JOZ

510(k)DeviceApplicantDecision
K191364T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL…JOZ · Traditional Fujimori Kogyo, Co., Ltd.02/14/2020SE
K181777AggreGuide A-100 ADPJOZ · Traditional Aggredyne, Inc.03/29/2019SE
K163274AggreGuide A-100 AA Assay, AggreGuide A-100 InstrumentJOZ · Special Aggredyne, Inc.04/05/2017SE
K161329Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channelJOZ · Special Chrono-Log Corp.12/02/2016SE
K141427Accumetrics,Inc. Verifynow Prutest, Accumetrics, Inc. Verifynow PrutestJOZ · Traditional Accumetrics, Inc.07/24/2015SE
K140893Cora (Coagulation Resonance Analysis) System with Platelet Mapping AssayJOZ · Traditional Coramed Technologies, LLC01/03/2015SE
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

More from Chrono-Log Corp.

510(k)DeviceDecision
K161329Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channelJOZ · Special 12/02/2016SE
K050265Chrono-Log Whole Blood Lumi-Aggregometer, Model 700JOZ · Traditional 10/14/2005SE
K032951Chrono-Log Whole Blood Aggregometer, Models 591A and 592AJOZ · Traditional 04/02/2004SE
K962426Chrono-Log Whole Blood Aggregometer (Wba) 591/592JOZ · Traditional 10/22/1996SE
K945414Ristocetin Cofactor Assay KitGGP · Traditional 01/11/1995SE
K940792Aggro/Link VW Cofactor SoftwareJOZ · Traditional 10/13/1994SE
K932566Aggro/Link Control SoftwareJBX · Traditional 11/02/1993SE
K922800Platelet Aggregation ReagentsGHR · Traditional 08/26/1992SE
K851025Aggro/Link Computer InterfaceJBX · Traditional 06/12/1985SE
K850592Platelet Aggregation ReagentJBX · Traditional 05/13/1985SE

Questions and answers

When was Reagent, Firefly #395 cleared by the FDA?

Reagent, Firefly #395 (K781807) received a 510(k) decision of Substantially Equivalent on November 22, 1978, 28 days after the submission was received.

What is the product code of K781807?

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