Multistat III Y GT Test

FDA 510(k) K771473 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK771473

Submission

Device name
Multistat III Y GT Test
Applicant
Instrumentation Laboratory CO
Mchenry, IL, US
Received
August 4, 1977
Decision date
September 13, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Instrumentation Laboratory CO

510(k)DeviceDecision
K233790Acl Top 970 CLJPA · Special 12/29/2023SE
K230852HemosIL Chromogenic Factor IXGGP · Traditional 12/13/2023SE
K221359ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgMJPA · Traditional 09/29/2023SE
K223608GEM Premier 7000 with IQM3CHL · Traditional 08/10/2023SE
K223187HemosIL Liquid Anti-XaQLU · Traditional 06/23/2023SE
K231031ACL TOP Family 70 SeriesGKP · Traditional 06/21/2023SE
K223090GEM Premier ChemSTATCGA · Special 01/27/2023SE
K223402HemosIL von Willebrand Factor AntigenGGP · Special 12/09/2022SE
K213464HemosIL Liquid Anti-XaKFF · Special 10/04/2022SE
K213426HemosIL ReadiPlasTinGJS · Traditional 08/16/2022SE

Questions and answers

When was Multistat III Y GT Test cleared by the FDA?

Multistat III Y GT Test (K771473) received a 510(k) decision of Substantially Equivalent on September 13, 1977, 40 days after the submission was received.