Il System 810, Acl and the Reagent Sets

FDA 510(k) K862301 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK862301

Submission

Device name
Il System 810, Acl and the Reagent Sets
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
June 17, 1986
Decision date
September 3, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GJA – Test, Thrombin Time
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7875
Specialty
Hematology

Other 510(k)s with product code GJA

510(k)DeviceApplicantDecision
K050817T-TekGJA · Traditional R2 Diagnostics, Inc.12/12/2005SE
K982209Accuclot Thrombin Time Reagent Model A8713/A4589GJA · Traditional Sigma Diagnostics, Inc.10/15/1998SE
K970645BC Thrombin ReagentGJA · Traditional Behring Diagnostics, Inc.05/19/1997SE
K925493Biomerieux Hemolab Thrombicalci-TestGJA · Traditional Biomerieux Vitek, Inc.04/21/1994SE
K930157Test ThrombinGJA · Traditional Behring Diagnostics, Inc.05/14/1993SE
K923220Thrombin Clot Time Test ProcedureGJA · Traditional Medical Laboratory Automation Systems, Inc.09/29/1992SE
K920147Thrombin Clotting Time ReagentGJA · Traditional Helena Laboratories05/01/1992SE
K900126TT and HNTT by HemochronGJA · Traditional International Technidyne Corp.02/05/1990SE
K894467Thrombin Time ReagentGJA · Traditional Sigma Chemical Co.09/05/1989SE
K884385Fibri-Prest/Thrombin-Prest ControlsGJA · Traditional American Bioproducts Co.12/28/1988SE

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Questions and answers

When was Il System 810, Acl and the Reagent Sets cleared by the FDA?

Il System 810, Acl and the Reagent Sets (K862301) received a 510(k) decision of Substantially Equivalent on September 3, 1986, 78 days after the submission was received.

What is the product code of K862301?

The FDA product code is GJA – Test, Thrombin Time, a Class II (moderate risk) device regulated under 21 CFR 864.7875.