Platelet-Trol II

FDA 510(k) K854353 · R&D Systems, Inc.

Substantially Equivalent

510(k) numberK854353

Submission

Device name
Platelet-Trol II
Applicant
R&D Systems, Inc.
Minneapolis, MN, US
Received
October 28, 1985
Decision date
November 26, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JPK – Mixture, Hematology Quality Control
Device class
Class II (moderate risk)
Regulation
21 CFR 864.8625
Specialty
Hematology

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More from R&D Systems, Inc.

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K160606BC-5D Hematology ControlJPK · Traditional 09/01/2016SE
K130962R&D 5D Retic Hematology ControlJPK · Special 07/24/2013SE
K101578R&D Systems Body Fluid-I Hematology ControlJPK · Traditional 04/28/2011SE
K100050R & D Systems Xeret Hematology ControlJPK · Special 01/29/2010SE
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K073178HCT Extended Hematology Control, Model HCT004JPK · Traditional 12/27/2007SE
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K072268HC WBC Hematology Control, Model: WBC00SJPK · Traditional 11/20/2007SE
K072096CBC-5D Plus Retics Hematology Control, Models: 5DR03, 5DR04JPK · Special 08/20/2007SE
K070334R&D Sickle QC ControlGGM · Traditional 03/29/2007SE

Questions and answers

When was Platelet-Trol II cleared by the FDA?

Platelet-Trol II (K854353) received a 510(k) decision of Substantially Equivalent on November 26, 1985, 29 days after the submission was received.

What is the product code of K854353?

The FDA product code is JPK – Mixture, Hematology Quality Control, a Class II (moderate risk) device regulated under 21 CFR 864.8625.