Hydragel 6 CSF Kit

FDA 510(k) K981048 · Morax

Substantially Equivalent

510(k) numberK981048

Submission

Device name
Hydragel 6 CSF Kit
Applicant
Morax
Chelsea, MI, US
Received
March 20, 1998
Decision date
October 7, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CFF – Immunoelectrophoretic, Immunoglobulins, (G, A, M)
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5510
Specialty
Immunology

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K991362Hydragel Hemoglobin(E), Mini Hemoglobin(E), 7 Hemoglobin(E), 15 Hemoglobin(E), Acid(E)…JBD · Traditional 06/21/1999SE
K990250Hydragel Ldl/Hdl Chol Direct Kit-P.N. 4005, Hydragel 7 Ldl/Hdl Chol Direct Kit-P.N.…LBT · Traditional 06/18/1999SE
K974854Hydragel-Mini Lipo Kit-Pn 4093, Hydragel Lipo Kit-Pn 4007, Hydragel Lipo Maxi Kit-Pn 4207JHO · Traditional 10/07/1998SE
K972591Hydragel Bence Jones Kit/Maxi Kit Hydragel Bence Jones/Hydragel 2/4 Bence Jones KitJKM · Traditional 03/04/1998SE
K972015Hydragel 7,15,30, Chol-Hdl KitLBT · Traditional 10/27/1997SE
K963844Hydragel 15 HB A1C KitLCP · Traditional 04/22/1997SE
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Questions and answers

When was Hydragel 6 CSF Kit cleared by the FDA?

Hydragel 6 CSF Kit (K981048) received a 510(k) decision of Substantially Equivalent on October 7, 1998, 201 days after the submission was received.

What is the product code of K981048?

The FDA product code is CFF – Immunoelectrophoretic, Immunoglobulins, (G, A, M), a Class II (moderate risk) device regulated under 21 CFR 866.5510.